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Items: 1 to 100 of 3381

VariationLocationGene(s)Protein changeCondition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr2:179470264
GRCh38:
Chr2:178605537
TTN, TTN-AS1T15352A, T16279A, T17920A, T8855A, T8980A, T9047AMyopathy, myofibrillar, 9, with early respiratory failureUncertain significance
(Jul 6, 2023)
criteria provided, single submitter
2.
GRCh37:
Chr2:179402218
GRCh38:
Chr2:178537491
LOC126806420, TTN, TTN-AS1N24174fs, N24299fs, N24366fs, N30671fs, N31598fs, N33239fsMyopathy, myofibrillar, 9, with early respiratory failureUncertain significance
(May 2, 2023)
criteria provided, single submitter
3.
GRCh37:
Chr2:179451375-179451376
GRCh38:
Chr2:178586648-178586649
TTN, TTN-AS1Y12353*, Y12478*, Y12545*, Y18850*, Y19777*, Y21418*Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy,
Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9, Myopathy, myofibrillar, 9, with early respiratory failure
Pathogenic
(Mar 30, 2021)
criteria provided, single submitter
4.
GRCh37:
Chr2:179485022
GRCh38:
Chr2:178620295
TTNV12841A, V13768A, V15409A, V6344A, V6469A, V6536ATibial muscular dystrophy, Dilated cardiomyopathy 1G, Hypertrophic cardiomyopathy 9,
Myopathy, myofibrillar, 9, with early respiratory failure, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy
Uncertain significance
(May 24, 2022)
criteria provided, single submitter
5.
GRCh37:
Chr2:179439315
GRCh38:
Chr2:178574588
TTN, TTN-AS1H14783Q, H14908Q, H14975Q, H21280Q, H22207Q, H23848QTibial muscular dystrophy, Dilated cardiomyopathy 1G, Myopathy, myofibrillar, 9, with early respiratory failure,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy, Hypertrophic cardiomyopathy 9
Uncertain significance
(Feb 5, 2021)
criteria provided, single submitter
6.
GRCh37:
Chr2:179413310
GRCh38:
Chr2:178548583
TTN, TTN-AS1D21950H, D22075H, D22142H, D28447H, D29374H, D31015HDilated cardiomyopathy 1G, Hypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy, Myopathy, myofibrillar, 9, with early respiratory failure
Uncertain significance
(Feb 5, 2021)
criteria provided, single submitter
7.
GRCh37:
Chr2:179413282
GRCh38:
Chr2:178548555
TTN, TTN-AS1T21959I, T22084I, T22151I, T28456I, T29383I, T31024IDilated cardiomyopathy 1G, Hypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy, Myopathy, myofibrillar, 9, with early respiratory failure
Uncertain significance
(Nov 3, 2022)
criteria provided, single submitter
8.
GRCh37:
Chr2:179547517
GRCh38:
Chr2:178682790
TTNE10684K, E11001K, E9757KDilated cardiomyopathy 1G, Hypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy, Myopathy, myofibrillar, 9, with early respiratory failure
Uncertain significance
(Oct 16, 2022)
criteria provided, single submitter
9.
GRCh37:
Chr2:179463358
GRCh38:
Chr2:178598631
TTN, TTN-AS1K10056Q, K10123Q, K16428Q, K17355Q, K18996Q, K9931QTibial muscular dystrophy, Dilated cardiomyopathy 1G, Hypertrophic cardiomyopathy 9,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy, Myopathy, myofibrillar, 9, with early respiratory failure
Uncertain significance
(Nov 9, 2022)
criteria provided, single submitter
10.
GRCh37:
Chr2:179543138
GRCh38:
Chr2:178678411
TTNTibial muscular dystrophy, Dilated cardiomyopathy 1G, Hypertrophic cardiomyopathy 9,
Myopathy, myofibrillar, 9, with early respiratory failure, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy
Uncertain significance
(Nov 8, 2022)
criteria provided, single submitter
11.
GRCh37:
Chr2:179635229
GRCh38:
Chr2:178770502
TTNL2718V, L2764VTibial muscular dystrophy, Dilated cardiomyopathy 1G, Hypertrophic cardiomyopathy 9,
Myopathy, myofibrillar, 9, with early respiratory failure, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy
Uncertain significance
(Oct 16, 2022)
criteria provided, single submitter
12.
GRCh37:
Chr2:179472915-179472916
GRCh38:
Chr2:178608188-178608189
LOC126806425, TTN, TTN-AS1H14997fs, H15924fs, H17565fs, H8500fs, H8625fs, H8692fsTibial muscular dystrophy, Dilated cardiomyopathy 1G, Hypertrophic cardiomyopathy 9,
Myopathy, myofibrillar, 9, with early respiratory failure, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy
Likely pathogenic
(Sep 12, 2022)
criteria provided, single submitter
13.
GRCh37:
Chr2:179615979
GRCh38:
Chr2:178751252
TTNK3716NTibial muscular dystrophy, Hypertrophic cardiomyopathy 9, Dilated cardiomyopathy 1G,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Myopathy, myofibrillar, 9, with early respiratory failure, Early-onset myopathy with fatal cardiomyopathy
Uncertain significance
(Nov 8, 2022)
criteria provided, single submitter
14.
GRCh37:
Chr2:179402563
GRCh38:
Chr2:178537836
TTN, TTN-AS1I24059T, I24184T, I24251T, I30556T, I31483T, I33124TTibial muscular dystrophy, Dilated cardiomyopathy 1G, Hypertrophic cardiomyopathy 9,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy, Myopathy, myofibrillar, 9, with early respiratory failure
Uncertain significance
(Nov 7, 2022)
criteria provided, single submitter
15.
GRCh37:
Chr2:179423372
GRCh38:
Chr2:178558645
TTN, TTN-AS1Dilated cardiomyopathy 1G, Hypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy, Myopathy, myofibrillar, 9, with early respiratory failure
Uncertain significance
(Mar 5, 2021)
criteria provided, single submitter
16.
GRCh37:
Chr2:179424403
GRCh38:
Chr2:178559676
TTN, TTN-AS1D19754A, D19879A, D19946A, D26251A, D27178A, D28819AMyopathy, myofibrillar, 9, with early respiratory failureUncertain significance
(Feb 10, 2022)
criteria provided, single submitter
17.
GRCh37:
Chr2:179537139
GRCh38:
Chr2:178672412
TTNA10341V, A11268V, A11642VHypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
not specified
Uncertain significance
(May 17, 2022)
criteria provided, multiple submitters, no conflicts
18.
GRCh37:
Chr2:179463253-179463255
GRCh38:
Chr2:178598526-178598528
TTN, TTN-AS1E10090del, E10157del, E16462del, E17389del, E19030del, E9965delnot provided, Cardiovascular phenotype, Hypertrophic cardiomyopathy 9,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Myopathy, myofibrillar, 9, with early respiratory failure,
Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy
Uncertain significance
(Jan 11, 2023)
criteria provided, multiple submitters, no conflicts
19.
GRCh37:
Chr2:179586618
GRCh38:
Chr2:178721891
TTNN6347S, N7274S, N7591SHypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
not provided
Uncertain significance
(Oct 17, 2022)
criteria provided, multiple submitters, no conflicts
20.
GRCh37:
Chr2:179457902
GRCh38:
Chr2:178593175
TTN, TTN-AS1I10613T, I10738T, I10805T, I17110T, I18037T, I19678TCardiovascular phenotype, Hypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Dilated cardiomyopathy 1G, Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy,
Early-onset myopathy with fatal cardiomyopathy, not provided
Uncertain significance
(Aug 11, 2021)
criteria provided, multiple submitters, no conflicts
21.
GRCh37:
Chr2:179407647
GRCh38:
Chr2:178542920
LOC126806421, TTN, TTN-AS1P23247S, P23372S, P23439S, P29744S, P30671S, P32312SCardiovascular phenotype, Hypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Dilated cardiomyopathy 1G, Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy,
Early-onset myopathy with fatal cardiomyopathy, not provided
Uncertain significance
(Oct 17, 2022)
criteria provided, multiple submitters, no conflicts
22.
GRCh37:
Chr2:179530473
GRCh38:
Chr2:178665746
TTNM11974THypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
See cases
Uncertain significance
(Oct 13, 2021)
criteria provided, multiple submitters, no conflicts
23.
GRCh37:
Chr2:179433674
GRCh38:
Chr2:178568947
TTN, TTN-AS1K16664*, K16789*, K16856*, K23161*, K24088*, K25729*Hypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
not provided
Likely pathogenic
(Nov 20, 2021)
criteria provided, multiple submitters, no conflicts
24.
GRCh37:
Chr2:179526697-179526698
GRCh38:
Chr2:178661970-178661971
TTNP12394fsHypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
not provided, Autosomal recessive limb-girdle muscular dystrophy type 2J
Uncertain significance
(May 2, 2023)
criteria provided, multiple submitters, no conflicts
25.
GRCh37:
Chr2:179611475
GRCh38:
Chr2:178746748
TTNR5218*Hypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
not provided
Uncertain significance
(Mar 1, 2022)
criteria provided, multiple submitters, no conflicts
26.
GRCh37:
Chr2:179412826
GRCh38:
Chr2:178548099
TTN, TTN-AS1L22111P, L22236P, L22303P, L28608P, L29535P, L31176PHypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
not provided
Uncertain significance
(Feb 17, 2022)
criteria provided, multiple submitters, no conflicts
27.
GRCh37:
Chr2:179529607-179529610
GRCh38:
Chr2:178664880-178664883
TTNS12030fsHypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
not provided
Conflicting interpretations of pathogenicity
(May 20, 2022)
criteria provided, conflicting interpretations
28.
GRCh37:
Chr2:179613376-179613379
GRCh38:
Chr2:178748649-178748652
TTNI4583fsHypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
not provided
Uncertain significance
(Nov 18, 2021)
criteria provided, multiple submitters, no conflicts
29.
GRCh37:
Chr2:179457606
GRCh38:
Chr2:178592879
TTN, TTN-AS1L10682R, L10807R, L10874R, L17179R, L18106R, L19747RHypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
not provided
Uncertain significance
(Sep 29, 2021)
criteria provided, multiple submitters, no conflicts
30.
GRCh37:
Chr2:179422738
GRCh38:
Chr2:178558011
TTN, TTN-AS1Y20050H, Y20175H, Y20242H, Y26547H, Y27474H, Y29115Hnot provided, Hypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Dilated cardiomyopathy 1G, Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy,
Early-onset myopathy with fatal cardiomyopathy
Uncertain significance
(Oct 21, 2021)
criteria provided, multiple submitters, no conflicts
31.
GRCh37:
Chr2:179659159-179659164
GRCh38:
Chr2:178794432-178794437
TTNHypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
not provided
Uncertain significance
(Aug 13, 2021)
criteria provided, multiple submitters, no conflicts
32.
GRCh37:
Chr2:179528341
GRCh38:
Chr2:178663614
TTNAutosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Hypertrophic cardiomyopathy 9,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Myopathy, myofibrillar, 9, with early respiratory failure,
Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy
Likely benign
(Mar 8, 2022)
criteria provided, multiple submitters, no conflicts
33.
GRCh37:
Chr2:179444129
GRCh38:
Chr2:178579402
LOC126806423, TTN, TTN-AS1Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Myopathy, myofibrillar, 9, with early respiratory failure, Early-onset myopathy with fatal cardiomyopathy, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9
Benign/Likely benign
(Mar 18, 2022)
criteria provided, multiple submitters, no conflicts
34.
GRCh37:
Chr2:179416007
GRCh38:
Chr2:178551280
TTN, TTN-AS1Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Myopathy, myofibrillar, 9, with early respiratory failure, Early-onset myopathy with fatal cardiomyopathy, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9
Likely benign
(Oct 17, 2022)
criteria provided, multiple submitters, no conflicts
35.
GRCh37:
Chr2:179407064
GRCh38:
Chr2:178542337
TTN, TTN-AS1Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Myopathy, myofibrillar, 9, with early respiratory failure, Early-onset myopathy with fatal cardiomyopathy, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9
Likely benign
(Mar 21, 2022)
criteria provided, multiple submitters, no conflicts
36.
GRCh37:
Chr2:179448344
GRCh38:
Chr2:178583617
TTN, TTN-AS1Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Myopathy, myofibrillar, 9, with early respiratory failure, Early-onset myopathy with fatal cardiomyopathy, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9
Likely benign
(Jul 19, 2022)
criteria provided, multiple submitters, no conflicts
37.
GRCh37:
Chr2:179456250
GRCh38:
Chr2:178591523
TTN, TTN-AS1Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy,
Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Tibial muscular dystrophy,
Hypertrophic cardiomyopathy 9, Myopathy, myofibrillar, 9, with early respiratory failure
Likely benign
(May 21, 2022)
criteria provided, multiple submitters, no conflicts
38.
GRCh37:
Chr2:179426226
GRCh38:
Chr2:178561499
TTN, TTN-AS1Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy,
Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Tibial muscular dystrophy,
Hypertrophic cardiomyopathy 9, Myopathy, myofibrillar, 9, with early respiratory failure
Likely benign
(Aug 23, 2022)
criteria provided, multiple submitters, no conflicts
39.
GRCh37:
Chr2:179513965
GRCh38:
Chr2:178649238
TTNDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy,
Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Tibial muscular dystrophy,
Hypertrophic cardiomyopathy 9, Myopathy, myofibrillar, 9, with early respiratory failure
Likely benign
(May 11, 2022)
criteria provided, multiple submitters, no conflicts
40.
GRCh37:
Chr2:179641867
GRCh38:
Chr2:178777140
LOC101927055, TTNDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9,
Myopathy, myofibrillar, 9, with early respiratory failure, Early-onset myopathy with fatal cardiomyopathy
Likely benign
(Apr 13, 2022)
criteria provided, multiple submitters, no conflicts
41.
GRCh37:
Chr2:179518250
GRCh38:
Chr2:178653523
TTNDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9,
Myopathy, myofibrillar, 9, with early respiratory failure, Early-onset myopathy with fatal cardiomyopathy
Likely benign
(Aug 21, 2022)
criteria provided, multiple submitters, no conflicts
42.
GRCh37:
Chr2:179446371
GRCh38:
Chr2:178581644
TTN, TTN-AS1Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Tibial muscular dystrophy,
Hypertrophic cardiomyopathy 9, Myopathy, myofibrillar, 9, with early respiratory failure, Early-onset myopathy with fatal cardiomyopathy,
Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J
Likely benign
(Nov 29, 2021)
criteria provided, multiple submitters, no conflicts
43.
GRCh37:
Chr2:179537449
GRCh38:
Chr2:178672722
TTNDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Early-onset myopathy with fatal cardiomyopathy, Myopathy, myofibrillar, 9, with early respiratory failure
Benign/Likely benign
(Jun 1, 2022)
criteria provided, multiple submitters, no conflicts
44.
GRCh37:
Chr2:179400587
GRCh38:
Chr2:178535860
TTN, TTN-AS1Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Early-onset myopathy with fatal cardiomyopathy, Myopathy, myofibrillar, 9, with early respiratory failure
Benign/Likely benign
(Sep 27, 2022)
criteria provided, multiple submitters, no conflicts
45.
GRCh37:
Chr2:179567200
GRCh38:
Chr2:178702473
TTNDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Early-onset myopathy with fatal cardiomyopathy, Myopathy, myofibrillar, 9, with early respiratory failure
Likely benign
(Oct 26, 2022)
criteria provided, multiple submitters, no conflicts
46.
GRCh37:
Chr2:179537446
GRCh38:
Chr2:178672719
TTNDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Early-onset myopathy with fatal cardiomyopathy, Myopathy, myofibrillar, 9, with early respiratory failure
Likely benign
(Aug 23, 2021)
criteria provided, multiple submitters, no conflicts
47.
GRCh37:
Chr2:179528838
GRCh38:
Chr2:178664111
TTNAutosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Myopathy, myofibrillar, 9, with early respiratory failure,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy, Dilated cardiomyopathy 1G,
Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9
Likely benign
(Oct 25, 2022)
criteria provided, multiple submitters, no conflicts
48.
GRCh37:
Chr2:179582497
GRCh38:
Chr2:178717770
TTNAutosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G, Myopathy, myofibrillar, 9, with early respiratory failure,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy, Dilated cardiomyopathy 1G,
Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9
Likely benign
(Mar 12, 2022)
criteria provided, multiple submitters, no conflicts
49.
GRCh37:
Chr2:179392051-179392052
GRCh38:
Chr2:178527324-178527325
TTN, TTN-AS1Tibial muscular dystrophy, Dilated cardiomyopathy 1G, Myopathy, myofibrillar, 9, with early respiratory failure,
Hypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy,
Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J
Benign/Likely benign
(Oct 5, 2022)
criteria provided, multiple submitters, no conflicts
50.
GRCh37:
Chr2:179642597
GRCh38:
Chr2:178777870
LOC101927055, TTNTibial muscular dystrophy, Dilated cardiomyopathy 1G, Myopathy, myofibrillar, 9, with early respiratory failure,
Hypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy,
Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J
Likely benign
(Oct 19, 2022)
criteria provided, multiple submitters, no conflicts
51.
GRCh37:
Chr2:179529424
GRCh38:
Chr2:178664697
TTNDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Myopathy, myofibrillar, 9, with early respiratory failure, Early-onset myopathy with fatal cardiomyopathy
Likely benign
(Apr 15, 2022)
criteria provided, multiple submitters, no conflicts
52.
GRCh37:
Chr2:179401648-179401649
GRCh38:
Chr2:178536921-178536922
TTN-AS1, LOC126806420, TTNDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy, Tibial muscular dystrophy,
Myopathy, myofibrillar, 9, with early respiratory failure, Hypertrophic cardiomyopathy 9
Likely benign
(Aug 12, 2022)
criteria provided, multiple submitters, no conflicts
53.
GRCh37:
Chr2:179430479
GRCh38:
Chr2:178565752
TTN, TTN-AS1Q26794*, Q17921*, Q24226*, Q17854*, Q17729*, Q25153*Cardiovascular phenotype, Dilated cardiomyopathy 1G, Tibial muscular dystrophy,
Early-onset myopathy with fatal cardiomyopathy, Hypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Myopathy, myofibrillar, 9, with early respiratory failure, Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J
Pathogenic/Likely pathogenic
(Aug 28, 2021)
criteria provided, multiple submitters, no conflicts
54.
GRCh37:
Chr2:179586664-179586665
GRCh38:
Chr2:178721937-178721938
TTNK6332fs, K7259fs, K7576fsDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy, Hypertrophic cardiomyopathy 9,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Myopathy, myofibrillar, 9, with early respiratory failure
Uncertain significance
(Jun 27, 2022)
criteria provided, multiple submitters, no conflicts
55.
GRCh37:
Chr2:179586600-179586601
GRCh38:
Chr2:178721873-178721874
TTNM6353fs, M7280fs, M7597fsDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy, Hypertrophic cardiomyopathy 9,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Myopathy, myofibrillar, 9, with early respiratory failure
Uncertain significance
(Jan 16, 2022)
criteria provided, multiple submitters, no conflicts
56.
GRCh37:
Chr2:179659131
GRCh38:
Chr2:178794404
TTNE465*Cardiovascular phenotype, Dilated cardiomyopathy 1G, Myopathy, myofibrillar, 9, with early respiratory failure,
Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Early-onset myopathy with fatal cardiomyopathy, Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J
Uncertain significance
(Apr 1, 2022)
criteria provided, multiple submitters, no conflicts
57.
GRCh37:
Chr2:179455996-179455997
GRCh38:
Chr2:178591269-178591270
TTN, TTN-AS1T11212fs, T18511fs, T20152fs, T11087fs, T11279fs, T17584fsCardiovascular phenotype, Dilated cardiomyopathy 1G, Myopathy, myofibrillar, 9, with early respiratory failure,
Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Early-onset myopathy with fatal cardiomyopathy, Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J
Likely pathogenic
(Dec 30, 2022)
criteria provided, multiple submitters, no conflicts
58.
GRCh37:
Chr2:179396704
GRCh38:
Chr2:178531977
TTN, TTN-AS1E25815Q, E25940Q, E26007Q, E32312Q, E33239Q, E34880QDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy
Uncertain significance
(Oct 26, 2021)
criteria provided, multiple submitters, no conflicts
59.
GRCh37:
Chr2:179656926
GRCh38:
Chr2:178792199
TTNDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy
Uncertain significance
(Jul 28, 2021)
criteria provided, multiple submitters, no conflicts
60.
GRCh37:
Chr2:179400292
GRCh38:
Chr2:178535565
TTN, TTN-AS1L24619V, L24744V, L31116V, L33684V, L24811V, L32043VMyopathy, myofibrillar, 9, with early respiratory failure, Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Early-onset myopathy with fatal cardiomyopathy, Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9,
Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J
Uncertain significance
(Oct 1, 2022)
criteria provided, multiple submitters, no conflicts
61.
GRCh37:
Chr2:179396157
GRCh38:
Chr2:178531430
TTN, TTN-AS1Y32494S, Y26122S, Y26189S, Y35062S, Y33421S, Y25997SMyopathy, myofibrillar, 9, with early respiratory failure, Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Early-onset myopathy with fatal cardiomyopathy, Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9,
Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J
Uncertain significance
(Nov 17, 2021)
criteria provided, multiple submitters, no conflicts
62.
GRCh37:
Chr2:179494963
GRCh38:
Chr2:178630236
TTNDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Myopathy, myofibrillar, 9, with early respiratory failure,
Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy,
Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9, Cardiovascular phenotype
Uncertain significance
(Feb 7, 2022)
criteria provided, multiple submitters, no conflicts
63.
GRCh37:
Chr2:179408194
GRCh38:
Chr2:178543467
LOC126806421, TTN, TTN-AS1L23104P, L29601P, L30528P, L23229P, L23296P, L32169PDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Myopathy, myofibrillar, 9, with early respiratory failure,
Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy,
Tibial muscular dystrophy, Hypertrophic cardiomyopathy 9
Uncertain significance
(Jun 20, 2022)
criteria provided, multiple submitters, no conflicts
64.
GRCh37:
Chr2:179544784
GRCh38:
Chr2:178680057
TTNDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Myopathy, myofibrillar, 9, with early respiratory failure,
Hypertrophic cardiomyopathy 9, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, not provided
Uncertain significance
(Oct 8, 2022)
criteria provided, multiple submitters, no conflicts
65.
GRCh37:
Chr2:179603863
GRCh38:
Chr2:178739136
TTNDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Myopathy, myofibrillar, 9, with early respiratory failure,
Early-onset myopathy with fatal cardiomyopathy, Tibial muscular dystrophy, Dilated cardiomyopathy 1G,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Hypertrophic cardiomyopathy 9
Uncertain significance
(Mar 14, 2022)
criteria provided, multiple submitters, no conflicts
66.
GRCh37:
Chr2:179393572
GRCh38:
Chr2:178528845
TTN, TTN-AS1V26571M, V26763M, V33068M, V33995M, V26696M, V35636MCardiovascular phenotype, Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Myopathy, myofibrillar, 9, with early respiratory failure, Early-onset myopathy with fatal cardiomyopathy, Tibial muscular dystrophy,
Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Hypertrophic cardiomyopathy 9
Uncertain significance
(May 14, 2022)
criteria provided, multiple submitters, no conflicts
67.
GRCh37:
Chr2:179395390
GRCh38:
Chr2:178530663
TTN, TTN-AS1T26378S, T35318S, T26253S, T32750S, T26445S, T33677SDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Myopathy, myofibrillar, 9, with early respiratory failure,
Early-onset myopathy with fatal cardiomyopathy, Tibial muscular dystrophy, Dilated cardiomyopathy 1G,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Hypertrophic cardiomyopathy 9
Uncertain significance
(Feb 25, 2022)
criteria provided, multiple submitters, no conflicts
68.
GRCh37:
Chr2:179397280
GRCh38:
Chr2:178532553
TTN, TTN-AS1E25748Q, E33047Q, E25623Q, E32120Q, E34688Q, E25815QDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Cardiovascular phenotype,
Tibial muscular dystrophy, Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Myopathy, myofibrillar, 9, with early respiratory failure, Hypertrophic cardiomyopathy 9, Early-onset myopathy with fatal cardiomyopathy
Uncertain significance
(Jun 7, 2022)
criteria provided, multiple submitters, no conflicts
69.
GRCh37:
Chr2:179397184
GRCh38:
Chr2:178532457
TTN, TTN-AS1E25780K, E25847K, E33079K, E25655K, E32152K, E34720KDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Hypertrophic cardiomyopathy 9, Tibial muscular dystrophy, Myopathy, myofibrillar, 9, with early respiratory failure,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy
Uncertain significance
(Apr 6, 2022)
criteria provided, multiple submitters, no conflicts
70.
GRCh37:
Chr2:179399769
GRCh38:
Chr2:178535042
TTN, TTN-AS1V24918D, V24793D, V24985D, V31290D, V32217D, V33858DDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Hypertrophic cardiomyopathy 9, Tibial muscular dystrophy, Myopathy, myofibrillar, 9, with early respiratory failure,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy
Uncertain significance
(Sep 1, 2022)
criteria provided, multiple submitters, no conflicts
71.
GRCh37:
Chr2:179595834
GRCh38:
Chr2:178731107
LOC126806431, TTNT4609I, T5536I, T5853IDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy,
Tibial muscular dystrophy, Myopathy, myofibrillar, 9, with early respiratory failure, Hypertrophic cardiomyopathy 9,
not specified
Uncertain significance
(Jan 10, 2022)
criteria provided, multiple submitters, no conflicts
72.
GRCh37:
Chr2:179401101
GRCh38:
Chr2:178536374
TTN-AS1, TTNI24393T, I24518T, I24585T, I30890T, I31817T, I33458TDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy,
Tibial muscular dystrophy, Myopathy, myofibrillar, 9, with early respiratory failure, Hypertrophic cardiomyopathy 9,
not provided
Uncertain significance
(Jan 12, 2022)
criteria provided, multiple submitters, no conflicts
73.
GRCh37:
Chr2:179428139
GRCh38:
Chr2:178563412
TTN, TTN-AS1P18509S, P18634S, P18701S, P25006S, P25933S, P27574SMyopathy, myofibrillar, 9, with early respiratory failureUncertain significance
(Mar 31, 2021)
criteria provided, single submitter
74.
GRCh37:
Chr2:179436487
GRCh38:
Chr2:178571760
TTN, TTN-AS1T15726I, T15851I, T15918I, T22223I, T23150I, T24791IHypertrophic cardiomyopathy 9, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Tibial muscular dystrophy, Myopathy, myofibrillar, 9, with early respiratory failure, Early-onset myopathy with fatal cardiomyopathy,
not provided
Uncertain significance
(Nov 2, 2021)
criteria provided, multiple submitters, no conflicts
75.
GRCh37:
Chr2:179631161
GRCh38:
Chr2:178766434
TTNE3171A, E3217ACardiovascular phenotype, Cardiomyopathy, Dilated cardiomyopathy 1G,
Tibial muscular dystrophy, Myopathy, myofibrillar, 9, with early respiratory failure, Autosomal recessive limb-girdle muscular dystrophy type 2J,
Early-onset myopathy with fatal cardiomyopathy, Hypertrophic cardiomyopathy 9
Uncertain significance
(Feb 8, 2022)
criteria provided, multiple submitters, no conflicts
76.
GRCh37:
Chr2:179411444
GRCh38:
Chr2:178546717
TTN, TTN-AS1V22506M, V22631M, V22698M, V29003M, V29930M, V31571MCardiomyopathy, Dilated cardiomyopathy 1G, Tibial muscular dystrophy,
Myopathy, myofibrillar, 9, with early respiratory failure, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy,
Hypertrophic cardiomyopathy 9
Uncertain significance
(Sep 14, 2021)
criteria provided, multiple submitters, no conflicts
77.
GRCh37:
Chr2:179451913
GRCh38:
Chr2:178587186
TTN, TTN-AS1A12277G, A12402G, A12469G, A18774G, A19701G, A21342GCardiomyopathy, Dilated cardiomyopathy 1G, Tibial muscular dystrophy,
Myopathy, myofibrillar, 9, with early respiratory failure, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy,
Hypertrophic cardiomyopathy 9
Uncertain significance
(Jul 28, 2021)
criteria provided, multiple submitters, no conflicts
78.
GRCh37:
Chr2:179536900
GRCh38:
Chr2:178672173
TTNDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Cardiomyopathy,
Dilated cardiomyopathy 1G, Tibial muscular dystrophy, Myopathy, myofibrillar, 9, with early respiratory failure,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy, Hypertrophic cardiomyopathy 9
Likely benign
(Aug 25, 2022)
criteria provided, multiple submitters, no conflicts
79.
GRCh37:
Chr2:179540666
GRCh38:
Chr2:178675939
TTNE10206Q, E11133Q, E11479QEarly-onset myopathy with fatal cardiomyopathy, not provided, Cardiomyopathy,
Dilated cardiomyopathy 1G, Tibial muscular dystrophy, Myopathy, myofibrillar, 9, with early respiratory failure,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy, Hypertrophic cardiomyopathy 9
Uncertain significance
(May 20, 2022)
criteria provided, multiple submitters, no conflicts
80.
GRCh37:
Chr2:179617880
GRCh38:
Chr2:178753153
TTNI3398T, I3444T, I3523T, I3590T, I3761TCardiovascular phenotype, Dilated cardiomyopathy 1G, Hypertrophic cardiomyopathy 9,
Cardiomyopathy, Dilated cardiomyopathy 1G, Tibial muscular dystrophy,
Myopathy, myofibrillar, 9, with early respiratory failure, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy,
Hypertrophic cardiomyopathy 9
Conflicting interpretations of pathogenicity
(Oct 20, 2021)
criteria provided, conflicting interpretations
81.
GRCh37:
Chr2:179605976
GRCh38:
Chr2:178741249
TTNT3632I, T3678I, T3757I, T3824I, T3995Inot provided, Dilated cardiomyopathy 1G, Tibial muscular dystrophy,
Myopathy, myofibrillar, 9, with early respiratory failure, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy,
Hypertrophic cardiomyopathy 9
Uncertain significance
(Sep 16, 2021)
criteria provided, multiple submitters, no conflicts
82.
GRCh37:
Chr2:179560973
GRCh38:
Chr2:178696246
TTNS10276A, S9032A, S9959Anot provided, Dilated cardiomyopathy 1G, Tibial muscular dystrophy,
Myopathy, myofibrillar, 9, with early respiratory failure, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy,
Hypertrophic cardiomyopathy 9
Uncertain significance
(Apr 8, 2022)
criteria provided, multiple submitters, no conflicts
83.
GRCh37:
Chr2:179621176
GRCh38:
Chr2:178756449
TTNT3505M, T3676MDilated cardiomyopathy 1G, Tibial muscular dystrophy, Myopathy, myofibrillar, 9, with early respiratory failure,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy, Hypertrophic cardiomyopathy 9
Uncertain significance
(Sep 13, 2021)
criteria provided, single submitter
84.
GRCh37:
Chr2:179438469
GRCh38:
Chr2:178573742
TTN, TTN-AS1L15065F, L15190F, L15257F, L21562F, L22489F, L24130FDilated cardiomyopathy 1G, Tibial muscular dystrophy, Myopathy, myofibrillar, 9, with early respiratory failure,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy, Hypertrophic cardiomyopathy 9
not providedno assertion provided
85.
GRCh37:
Chr2:179442011
GRCh38:
Chr2:178577284
TTN, TTN-AS1Dilated cardiomyopathy 1G, Tibial muscular dystrophy, Myopathy, myofibrillar, 9, with early respiratory failure,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy, Hypertrophic cardiomyopathy 9
not providedno assertion provided
86.
GRCh37:
Chr2:179399700
GRCh38:
Chr2:178534973
TTN, TTN-AS1S24816*, S24941*, S25008*, S31313*, S32240*, S33881*not provided, Dilated cardiomyopathy 1G, Tibial muscular dystrophy,
Myopathy, myofibrillar, 9, with early respiratory failure, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy,
Hypertrophic cardiomyopathy 9
Likely pathogenic
(Mar 17, 2022)
criteria provided, multiple submitters, no conflicts
87.
GRCh37:
Chr2:179613014
GRCh38:
Chr2:178748287
LOC126806432, TTNR4705*not provided, Dilated cardiomyopathy 1G, Tibial muscular dystrophy,
Myopathy, myofibrillar, 9, with early respiratory failure, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy,
Hypertrophic cardiomyopathy 9
Uncertain significance
(Nov 5, 2021)
criteria provided, multiple submitters, no conflicts
88.
GRCh37:
Chr2:179438338
GRCh38:
Chr2:178573611
TTN, TTN-AS1A15109V, A15234V, A15301V, A21606V, A22533V, A24174Vnot provided, Dilated cardiomyopathy 1G, Tibial muscular dystrophy,
Myopathy, myofibrillar, 9, with early respiratory failure, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy,
Hypertrophic cardiomyopathy 9
Uncertain significance
(Apr 20, 2022)
criteria provided, multiple submitters, no conflicts
89.
GRCh37:
Chr2:179419222
GRCh38:
Chr2:178554495
TTN, TTN-AS1E20553K, E20678K, E20745K, E27050K, E27977K, E29618KCardiovascular phenotype, Dilated cardiomyopathy 1G, Tibial muscular dystrophy,
Myopathy, myofibrillar, 9, with early respiratory failure, Autosomal recessive limb-girdle muscular dystrophy type 2J, Early-onset myopathy with fatal cardiomyopathy,
Hypertrophic cardiomyopathy 9, not specified
Uncertain significance
(Oct 9, 2021)
criteria provided, multiple submitters, no conflicts
90.
GRCh37:
Chr2:179426737
GRCh38:
Chr2:178562010
TTN-AS1, TTNA18976V, A19101V, A19168V, A25473V, A26400V, A28041VDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Hypertrophic cardiomyopathy 9,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
not provided
Uncertain significance
(Dec 6, 2021)
criteria provided, multiple submitters, no conflicts
91.
GRCh37:
Chr2:179576833
GRCh38:
Chr2:178712106
TTND7998Y, D8925Y, D9242YDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Hypertrophic cardiomyopathy 9,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
not provided
Uncertain significance
(Jul 5, 2021)
criteria provided, multiple submitters, no conflicts
92.
GRCh37:
Chr2:179454138
GRCh38:
Chr2:178589411
TTN-AS1, TTND11707N, D11832N, D11899N, D18204N, D19131N, D20772NDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Hypertrophic cardiomyopathy 9,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
not provided
Uncertain significance
(Sep 1, 2021)
criteria provided, multiple submitters, no conflicts
93.
GRCh37:
Chr2:179514618-179514625
GRCh38:
Chr2:178649891-178649898
TTNDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Hypertrophic cardiomyopathy 9,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
not provided
Uncertain significance
(Oct 14, 2021)
criteria provided, multiple submitters, no conflicts
94.
GRCh37:
Chr2:179397075
GRCh38:
Chr2:178532348
TTN, TTN-AS1R25691T, R25816T, R25883T, R32188T, R33115T, R34756TDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Dilated cardiomyopathy 1G,
Autosomal recessive limb-girdle muscular dystrophy type 2J, Hypertrophic cardiomyopathy 9, Myopathy, myofibrillar, 9, with early respiratory failure,
Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy, not provided
Uncertain significance
(Apr 4, 2023)
criteria provided, multiple submitters, no conflicts
95.
GRCh37:
Chr2:179426512
GRCh38:
Chr2:178561785
TTN, TTN-AS1I19051T, I19176T, I19243T, I25548T, I26475T, I28116TDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Hypertrophic cardiomyopathy 9,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
not provided
Uncertain significance
(Aug 12, 2021)
criteria provided, multiple submitters, no conflicts
96.
GRCh37:
Chr2:179600391
GRCh38:
Chr2:178735664
TTNL3684F, L4611F, L4928FDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Hypertrophic cardiomyopathy 9,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
not provided
Uncertain significance
(Oct 1, 2021)
criteria provided, multiple submitters, no conflicts
97.
GRCh37:
Chr2:179453318
GRCh38:
Chr2:178588591
TTN, TTN-AS1G11980A, G12105A, G12172A, G18477A, G19404A, G21045ADilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Hypertrophic cardiomyopathy 9,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
not provided
Uncertain significance
(Oct 28, 2021)
criteria provided, multiple submitters, no conflicts
98.
GRCh37:
Chr2:179453260
GRCh38:
Chr2:178588533
TTN, TTN-AS1Dilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Hypertrophic cardiomyopathy 9,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
not provided
Uncertain significance
(Oct 9, 2021)
criteria provided, multiple submitters, no conflicts
99.
GRCh37:
Chr2:179634595
GRCh38:
Chr2:178769868
TTNV2859M, V2905MDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Hypertrophic cardiomyopathy 9,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
not provided
Uncertain significance
(Dec 28, 2021)
criteria provided, multiple submitters, no conflicts
100.
GRCh37:
Chr2:179402182
GRCh38:
Chr2:178537455
LOC126806420, TTN, TTN-AS1Y24186C, Y24311C, Y24378C, Y30683C, Y31610C, Y33251CDilated cardiomyopathy 1G, Autosomal recessive limb-girdle muscular dystrophy type 2J, Hypertrophic cardiomyopathy 9,
Myopathy, myofibrillar, 9, with early respiratory failure, Tibial muscular dystrophy, Early-onset myopathy with fatal cardiomyopathy,
not provided, Cardiovascular phenotype
Uncertain significance
(Oct 19, 2021)
criteria provided, multiple submitters, no conflicts
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