rs387906466(-;AAATC)
From SNPedia
| Carrier of a Hemophilia A mutation |
| Is a | genotype |
| of | rs387906466 |
| Gene | F8 |
| Chromosome | X |
| Position | 154,837,737 |
| mentioned | by |
| Magnitude | 3.5 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 5.5 | Hemophilia A (severity varies) |
| (-;AAATC) | 3.5 | Carrier of a Hemophilia A mutation |
| (AATCA;AATCA) | 0 | common in clinvar |
| (ATCAA;ATCAA) | 0 | common in clinvar |
| (I;I) | 0 | common genotype |
X-linked recessive, so females are generally unaffected in the absence of a second F8 gene mutation, however some females may experience clotting issues.
