| | LOC126806428, TTN (W5833* +2 more) | Single nucleotide variant (nonsense +1 more) | TTN-Related Disorders | |
| | TTN-AS1, TTN (T23951fs +5 more) | Insertion (non-coding transcript variant +1 more) | TTN-Related Disorders | |
| | TTN, TTN-AS1 (T13971fs +5 more) | Deletion (frameshift variant) | TTN-related condition | |
| | LOC126806429, TTN (C5496F +2 more) | Single nucleotide variant (missense variant +1 more) | TTN-related condition | |
| | | Deletion (nonsense) | TTN-related condition | |
| | TTN, TTN-AS1 (R18629G +5 more) | Single nucleotide variant (missense variant) | TTN-related condition | |
| | TTN, TTN-AS1 (E19195D +5 more) | Single nucleotide variant (missense variant) | TTN-related condition | |
| | | Single nucleotide variant (intron variant) | TTN-related condition | |
| | | Single nucleotide variant (synonymous variant) | TTN-related condition | |
| | | Single nucleotide variant (synonymous variant) | TTN-related condition | |
| | TTN, TTN-AS1 (L14147V +5 more) | Single nucleotide variant (missense variant) | TTN-related condition | |
| | LOC126806424, TTN +1 more (Y10847C +5 more) | Single nucleotide variant (missense variant) | TTN-related condition | |
| | | Single nucleotide variant (synonymous variant) | TTN-related condition | |
| | | Single nucleotide variant (intron variant) | TTN-related condition | |
| | TTN, TTN-AS1 (G20800S +5 more) | Single nucleotide variant (missense variant) | TTN-related condition | |
| | TTN, TTN-AS1 (P20403R +5 more) | Single nucleotide variant (missense variant) | TTN-related condition | |
| | | Single nucleotide variant (synonymous variant) | TTN-related condition | |
| | | Single nucleotide variant (synonymous variant) | TTN-related condition | |
| | | Single nucleotide variant (synonymous variant) | TTN-related condition | |
| | | Single nucleotide variant (synonymous variant) | TTN-related condition | |
| | | Single nucleotide variant (intron variant) | TTN-related condition | |
| | | Single nucleotide variant (synonymous variant) | TTN-related condition | |
| | | Single nucleotide variant (synonymous variant) | TTN-related condition | |
| | TTN, TTN-AS1 (S18880R +5 more) | Single nucleotide variant (missense variant) | TTN-related condition | |
| | | Single nucleotide variant (intron variant) | TTN-related condition | |
| | LOC126806427, TTN (R12606fs +5 more) | Microsatellite (frameshift variant) | TTN-related condition | |
| | | Single nucleotide variant (intron variant) | TTN-related condition | |
| | | Single nucleotide variant (synonymous variant) | TTN-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | TTN-related condition | |
| | TTN, TTN-AS1 (N14085Y +5 more) | Single nucleotide variant (missense variant) | TTN-related condition | |
| | LOC126806431, TTN (P4393L +2 more) | Single nucleotide variant (missense variant +1 more) | TTN-related condition | |
| | TTN, TTN-AS1 (E19401K +5 more) | Single nucleotide variant (missense variant) | TTN-related condition | |
| | TTN, TTN-AS1 (T12004A +5 more) | Single nucleotide variant (missense variant) | TTN-related condition | |
| | LOC126806431, TTN (D4645fs +2 more) | Deletion (frameshift variant +1 more) | TTN-related condition | |
| | TTN, TTN-AS1 (P26093K +5 more) | Indel (missense variant) | TTN-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | TTN-related condition | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | TTN-related condition | |
| | | Single nucleotide variant (synonymous variant) | TTN-related condition | |
| | LOC126806427, TTN (A12470G +5 more) | Single nucleotide variant (missense variant) | TTN-related condition | |
| | TTN, TTN-AS1 (V15768A +5 more) | Single nucleotide variant (missense variant) | TTN-related condition | |
| | | Single nucleotide variant (synonymous variant) | TTN-related condition | |
| | TTN, TTN-AS1 (L10004fs +5 more) | Deletion (frameshift variant) | Dilated cardiomyopathy 1G | |
| | LOC126806422, TTN +1 more (A14263V +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | LOC126806425, TTN +1 more (F15027V +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | TTN, TTN-AS1 (Q25537* +5 more) | Single nucleotide variant (nonsense) | not provided | |
| | LOC126806423, TTN +1 more (T13449S +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | TTN, TTN-AS1 (G26360R +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | TTN, TTN-AS1 (K15487E +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | TTN, TTN-AS1 (D23376fs +5 more) | Deletion (frameshift variant) | not provided | |
| | TTN, TTN-AS1 (A14942V +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126806422, TTN +1 more (D14256H +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | TTN, TTN-AS1 (Y22378C +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | TTN-AS1, TTN (S22929N +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | TTN, TTN-AS1 (G12622fs +5 more) | Deletion (frameshift variant) | not provided | |
| | TTN, TTN-AS1 (S12624R +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | TTN, TTN-AS1 (G18306R +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | TTN, TTN-AS1 (Y20504N +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | TTN, TTN-AS1 (W18425fs +5 more) | Insertion (frameshift variant) | not provided | |
| | TTN, TTN-AS1 (V15689A +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC101927055, TTN (P1388S +1 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | TTN, TTN-AS1 (P13518L +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | TTN, TTN-AS1 (D20437N +5 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | TTN, TTN-AS1 (V17770fs +5 more) | Deletion (frameshift variant) | Dilated cardiomyopathy 1G | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (V7696fs +5 more) | Deletion (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | LOC101927055, TTN (V1307fs +1 more) | Deletion (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (A32338fs +5 more) | Deletion (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (Y25090C +5 more) | Single nucleotide variant (missense variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (E17874* +5 more) | Duplication (nonsense) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (N22586fs +5 more) | Duplication (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (F6557fs +5 more) | Deletion (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (S14106fs +5 more) | Duplication (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (M26487L +5 more) | Single nucleotide variant (missense variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (K18286* +5 more) | Single nucleotide variant (nonsense) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | LOC126806422, TTN +1 more (P14307fs +5 more) | Deletion (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (T14724fs +5 more) | Duplication (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN, TTN-AS1 (A20876fs +5 more) | Microsatellite (frameshift variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | TTN-AS1, LOC126806422 +1 more | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (splice donor variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (intron variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal recessive limb-girdle muscular dystrophy type 2J +1 more | |