| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130056513, ZNF839 (L69R) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | LOC130056513, ZNF839 (D71G) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | LOC130056513, ZNF839 (Q74P) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
Click to view in NCBI Gene