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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH7
(A1241S)
Single nucleotide variant
(missense variant)
Myosin storage myopathy
+3 more
GUncertain significance
MYH7
(E1180A)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1S
+1 more
GUncertain significance
LOC126861898, MYH7
(E779K)
Single nucleotide variant
(missense variant)
Myosin storage myopathy
+1 more
GConflicting classifications of pathogenicity
MYH7
(A331T)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1S
GUncertain significance
MYH7
(R237W)
Single nucleotide variant
(missense variant)
not provided
+6 more
GConflicting classifications of pathogenicity
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