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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNT2
(I221T +5 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+8 more
GConflicting classifications of pathogenicity
TNNT2
(R151fs +3 more)
Deletion
(frameshift variant)
Cardiomyopathy
+6 more
GConflicting classifications of pathogenicity
TNNT2
(A104V +2 more)
Single nucleotide variant
(missense variant +1 more)
Hypertrophic cardiomyopathy
+6 more
GConflicting classifications of pathogenicity
TNNT2
(Q16K)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1D
GUncertain significance
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