| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126862493, MYH8
+1 more (E1838A) | Single nucleotide variant (missense variant) | Hecht syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | LOC126862494, MYH8
+1 more | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
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