| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861844, MYO16
+1 more (R1090S +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | LOC126861844, MYO16
+1 more (A1108S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861844, MYO16
+1 more (E1131K +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861844, MYO16
+1 more (R1110Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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