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Links from MedGen

Items: 1 to 100 of 229

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNC1
(M45I)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
GLikely pathogenic
TNNC1
(A22S)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
GUncertain significance
TNNC1
(D62Y)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
GUncertain significance
TNNC1
(I4M)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
GPathogenic
TNNC1
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
GPathogenic
TNNC1
Deletion
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
(K92I)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
Deletion
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
(E55fs)
Deletion
(frameshift variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
(K86T)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(T53I)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
(D105G)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(A22E)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
(D113E)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(D2V)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
(V72A)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(A108fs)
Deletion
(frameshift variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(L41M)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(E55K)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+2 more
GLikely benign
TNNC1
(D113fs)
Deletion
(frameshift variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(splice donor variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Duplication
(intron variant)
Hypertrophic cardiomyopathy 13
+1 more
GBenign
TNNC1
(M157V)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+2 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+2 more
GLikely benign
TNNC1
(D3G)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(N107K)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(D139A)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(T124P)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(I61M)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(E59K)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(G146R)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(G146C)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(E152K)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
GPathogenic
TNNC1
(M81I)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+3 more
GUncertain significance
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+2 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
not provided
+2 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+2 more
GLikely benign
TNNC1
Deletion
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GBenign
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+2 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
(L100F)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(A8G)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(G68S)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(G146S)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+2 more
GUncertain significance
TNNC1
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(M103I)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(M103L)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(R83W)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 13
+1 more
GUncertain significance
TNNC1
(E95D)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 13
+2 more
GUncertain significance
TNNC1
Indel
(nonsense)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GLikely benign
TNNC1
(K158R)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(K118N)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(Q122fs)
Duplication
(frameshift variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(splice donor variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(Y5C)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(M157R)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
(S89G)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GLikely benign
TNNC1
(R83Q)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+1 more
GUncertain significance
TNNC1
Single nucleotide variant
(intron variant)
not specified
+2 more
GUncertain significance
TNNC1
(I112V)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1Z
+2 more
GUncertain significance
TNNC1
Single nucleotide variant
(synonymous variant)
Hypertrophic cardiomyopathy 13
+1 more
GLikely benign
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