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Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNT2
(R286C +5 more)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1D
+7 more
GConflicting classifications of pathogenicity
TNNT2
(R278P +5 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 2
+6 more
GConflicting classifications of pathogenicity
TNNT2
(R278H +5 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+6 more
GConflicting classifications of pathogenicity
TNNT2
(R278C +5 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 2
+9 more
GConflicting classifications of pathogenicity
TNNT2
(V218L +5 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
TNNT2
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1D
+5 more
GConflicting classifications of pathogenicity
TNNT2
(N164K +3 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GUncertain significance
TNNT2
(N150K +3 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 1
GUncertain significance
TNNT2
(F110L +2 more)
Single nucleotide variant
(missense variant +1 more)
Dilated cardiomyopathy 1D
+7 more
GPathogenic/Likely pathogenic
TNNT2
(A104V +2 more)
Single nucleotide variant
(missense variant +1 more)
Dilated cardiomyopathy 1D
+6 more
GConflicting classifications of pathogenicity
TNNT2
(A36P +2 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+7 more
GConflicting classifications of pathogenicity
TNNT2
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy
+6 more
GBenign
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