rs137852283(G;G)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs137852283 |
| Gene | F9 |
| Chromosome | X |
| Position | 139,561,836 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 5.5 | Hemophilia B (severity varies) |
| (C;G) | 3.5 | Carrier of a Hemophilia B mutation |
| (G;G) | 0 | common in clinvar |
| (G;T) | 3.5 | Carrier of a Hemophilia B mutation |
| (T;T) | 5.5 | Hemophilia B (severity varies) |
