| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130058849, ZNF785 (V36A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130058849, ZNF785 (P9Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130058849, ZNF785 (P3Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene