| | LOC129931031, SLC30A7 (P13L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129931031, SLC30A7 (G24D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129931032, SLC30A7 (S28A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129931032, SLC30A7 (L30P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | DPH5, SLC30A7 (I7V +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | SLC30A7, DPH5 (I9L +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | DPH5, SLC30A7 (G257S +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | DPH5, SLC30A7 (T236P +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | SLC30A7, DPH5 (S44A +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |