rs104894835(A;G)
From SNPedia
| Carrier of a Fabry disease mutation; X-linked so risk is to sons |
| Is a | genotype |
| of | rs104894835 |
| Gene | GLA, RPL36A-HNRNPH2, HNRNPH2 |
| Chromosome | X |
| Position | 101,407,803 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| (A;G) | 3 | Carrier of a Fabry disease mutation; X-linked so risk is to sons |
| (G;G) | 6 | Fabry disease |
Mostly unaffected in absence of a second GLA gene mutation; see text and links via main rs-page
