rs137852260(C;T)
From SNPedia
| Carrier of a Hemophilia B mutation |
| Is a | genotype |
| of | rs137852260 |
| Gene | F9 |
| Chromosome | X |
| Position | 139,561,829 |
| mentioned | by |
| Magnitude | 3.5 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 5.5 | Hemophilia B (severity varies) |
| (C;T) | 3.5 | Carrier of a Hemophilia B mutation |
| (T;T) | 0 | common in clinvar |
X-linked recessive, so females are generally unaffected in the absence of a second F9 gene mutation, however some females may experience clotting issues.
