rs137852268(C;T)
From SNPedia
Carrier of a Hemophilia B mutation |
Is a | genotype |
of | rs137852268 |
Gene | F9 |
Chromosome | X |
Position | 139,562,013 |
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.