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Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNI3, TNNT1
(E12G)
Single nucleotide variant
(missense variant)
Dilated Cardiomyopathy, Recessive
+5 more
GBenign/Likely benign
TNNI3
Single nucleotide variant
(intron variant)
not specified
+3 more
GBenign/Likely benign
TNNI3
Single nucleotide variant
(synonymous variant)
Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome
+8 more
GConflicting classifications of pathogenicity
TNNI3
(P82S)
Single nucleotide variant
(missense variant)
Familial restrictive cardiomyopathy
+12 more
GBenign/Likely benign
TNNI3
Deletion
(intron variant)
Dilated Cardiomyopathy, Recessive
+6 more
GConflicting classifications of pathogenicity
DNAAF3, DNAAF3-AS1
+1 more
(G224S +3 more)
Single nucleotide variant
(missense variant)
Dilated Cardiomyopathy, Recessive
+6 more
GBenign/Likely benign
DNAAF3, DNAAF3-AS1
+1 more
Single nucleotide variant
(synonymous variant)
Dilated Cardiomyopathy, Recessive
+6 more
GBenign/Likely benign
DNAAF3, DNAAF3-AS1
+1 more
Single nucleotide variant
(synonymous variant)
Dilated Cardiomyopathy, Recessive
+6 more
GBenign/Likely benign
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