| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126862123, SLC12A1 (A600V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862123, SLC12A1 (T631S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862123, SLC12A1 (Y632H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene