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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CSRP3
(R146H +1 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+4 more
GUncertain significance
MYBPC3
(S928L)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+7 more
GUncertain significance
ABCC9
(E960Q +1 more)
Single nucleotide variant
(missense variant)
Prolonged QT interval
GUncertain significance
MYH7
(N1824S)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+6 more
GUncertain significance
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