| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126861844, MYO16 +1 more (R1100H +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126861844, MYO16 +1 more | Duplication (splice donor variant) | not provided | |
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