| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (5 prime UTR variant +2 more) | SLC9A6-related disorder +1 more | |
| | LOC130068746, SLC9A6 (R3W) | Single nucleotide variant (missense variant +1 more) | Christianson syndrome +1 more | |
| | LOC130068746, SLC9A6 (A9S) | Single nucleotide variant (missense variant +1 more) | Christianson syndrome | |
Click to view in NCBI Gene