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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH2, MYHAS
(L1877P)
Single nucleotide variant
(missense variant)
Myopathy, proximal, and ophthalmoplegia
GPathogenic/Likely pathogenic
MYH2, MYHAS
(N1731S)
Single nucleotide variant
(missense variant)
Myopathy, proximal, and ophthalmoplegia
GUncertain significance
MYH2, MYHAS
(A1336V)
Single nucleotide variant
(missense variant)
Myopathy, proximal, and ophthalmoplegia
+1 more
GUncertain significance
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