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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNT2
(K253R +5 more)
Single nucleotide variant
(missense variant)
Dilated Cardiomyopathy, Dominant
+11 more
GBenign/Likely benign
TNNT2
(D249N +5 more)
Single nucleotide variant
(missense variant)
not provided
+5 more
GUncertain significance
TNNT2
(Y241C +5 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GUncertain significance
TNNT2
(L178F +3 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 2
+4 more
GUncertain significance
TNNT2
(R134W +2 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
+6 more
GConflicting classifications of pathogenicity
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