| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | ZNF765-ZNF761, ZNF761 (I15V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ZNF761, ZNF765-ZNF761 (E16A) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ZNF765-ZNF761, ZNF761 (E57K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF761, ZNF765-ZNF761 (K92R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF765-ZNF761, ZNF761 (F279C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF761, ZNF765-ZNF761 (K478R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF761, ZNF765-ZNF761 (L705V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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