rs104894342(A;G)
From SNPedia
| Carrier of a tumoral calcinosis mutation |
| Is a | genotype |
| of | rs104894342 |
| Gene | FGF23 |
| Chromosome | 12 |
| Position | 4,379,372 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| (A;G) | 3 | Carrier of a tumoral calcinosis mutation |
Unaffected in absence of a second FGF23 gene mutation; see text via main rs-page.
