| | ZHX1-C8orf76, C8orf76 (F8V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ZHX1-C8orf76, ZHX1 (R866W) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ZHX1, ZHX1-C8orf76 (R761T) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ZHX1, ZHX1-C8orf76 (R751W) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ZHX1, ZHX1-C8orf76 (P656R) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ZHX1, ZHX1-C8orf76 (V592A) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ZHX1, ZHX1-C8orf76 (M498T) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ZHX1-C8orf76, ZHX1 (P442L) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ZHX1-C8orf76, ZHX1 (T437A) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ZHX1, ZHX1-C8orf76 (A434T) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ZHX1, ZHX1-C8orf76 (M311V) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ZHX1, ZHX1-C8orf76 (N284S) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ZHX1, ZHX1-C8orf76 (P244T) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ZHX1-C8orf76, ZHX1 (I238V) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ZHX1, ZHX1-C8orf76 (S235G) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ZHX1, ZHX1-C8orf76 (P216R) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ZHX1-C8orf76, ZHX1 (N162Y) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ZHX1, ZHX1-C8orf76 (I148V) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |