rs387906449(-;AA)
From SNPedia
| Carrier of a Hemophilia A mutation |
| Is a | genotype |
| of | rs387906449 |
| Gene | F8 |
| Chromosome | X |
| Position | 154,930,241 |
| mentioned | by |
| Magnitude | 3.5 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 5.5 | Hemophilia A (severity varies) |
| (-;AA) | 3.5 | Carrier of a Hemophilia A mutation |
| (AA;AA) | 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.
