rs137852386(G;T)
From SNPedia
| Carrier of a Hemophilia A mutation |
| Is a | genotype |
| of | rs137852386 |
| Gene | F8 |
| Chromosome | X |
| Position | 154,997,011 |
| Merged from | Rs28935208 |
| mentioned | by |
| Magnitude | 3.5 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (G;T) | 3.5 | Carrier of a Hemophilia A mutation |
| (T;T) | 0 | common in clinvar |
X-linked recessive, so females are generally unaffected in the absence of a second F8 gene mutation, however some females may experience clotting issues.
