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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH7
(E1223K)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+11 more
GConflicting classifications of pathogenicity
MYH7
(F494L)
Single nucleotide variant
(missense variant)
Myosin storage myopathy
GUncertain significance
MYH7
(R369Q)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
GLikely pathogenic
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