| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130003098, SLC34A3 (A585T) | Single nucleotide variant (missense variant) | Autosomal recessive hypophosphatemic bone disease +2 more | |
| | LOC130003098, SLC34A3 (A595P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene