rs121908525(C;T)
From SNPedia
| Carrier of a type I primary hyperoxaluria mutation |
| Is a | genotype |
| of | rs121908525 |
| Gene | AGXT |
| Chromosome | 2 |
| Position | 240,875,159 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (C;T) | 3 | Carrier of a type I primary hyperoxaluria mutation |
| (T;T) | 0 | common in clinvar |
Unaffected in absence of a second AGXT gene mutation
