| | ADH4, LOC100507053 (L367V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADH4, LOC100507053 (I298T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADH4, LOC100507053 (F235L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADH4, LOC100507053 (N231S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADH4, LOC100507053 (A241T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADH4, LOC100507053 (L230P +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADH4, LOC100507053 (I111T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADH4, LOC100507053 (P106R +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADH4, LOC100507053 (V85I +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADH4, LOC100507053 (A72V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADH4, LOC100507053 (H88R +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC100507053, ADH4 (A62P +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC100507053, ADH4 (K52E +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADH4, LOC100507053 (P32L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC100507053, ADH4 (E28K +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC100507053, ADH4 (P21A +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |