| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130059257, SLC12A4 (C27F) | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
| | LOC130059257, SLC12A4 (G13R) | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene