| | | 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) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ABCB4, CROT (P214T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ABCB4, CROT (H253L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CROT, ABCB4 (A266T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ABCB4, CROT (R280Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CROT, ABCB4 (D287A +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CROT, ABCB4 (S272N +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CROT, ABCB4 (G307D +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ABCB4, CROT (Y341H +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ABCB4, CROT (D371N +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CROT, ABCB4 (I346S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CROT, ABCB4 (I371T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CROT, ABCB4 (L414I +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CROT, ABCB4 (R479H +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CROT, ABCB4 (E481D +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ABCB4, CROT (V460L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CROT, ABCB4 (E506G +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ABCB4, CROT (L540F +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ABCB4, CROT (E516G +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CROT, ABCB4 (V546F +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |