| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126862497, MYH1
+1 more (R1913W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862497, MYH1
+1 more (E1909Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862497, MYH1
+1 more (H1905N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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