| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126861702, ZNF10 (Q135H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861702, ZNF10 (V163D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861702, ZNF10 (K168T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861702, ZNF10 (P176S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861702, ZNF10 (R188H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF10, LOC126861702 (N211S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861702, ZNF10 (D242G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861702, ZNF10 (L247F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861702, ZNF10 (E266D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861702, ZNF10 (P292L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene