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.