rs137852283(C;G)

Carrier of a Hemophilia B mutation

Magnitude
3.5Important
Repute
Bad
On SNPedia
rs137852283(C;G)
Gene
F9

Other genotypes of rs137852283

  1. C;CMost notableBadHemophilia B (severity varies)Very important · 5.5
  2. G;GGoodcommon in clinvarTypical · 0.0
  3. G;TBadCarrier of a Hemophilia B mutationImportant · 3.5
  4. T;TBadHemophilia B (severity varies)Very important · 5.5

All about rs137852283

Notes

From SNPedia

X-linked recessive, so females are generally unaffected in the absence of a second F9 gene mutation, however some females may experience clotting issues.

Source and license

Adapted from rs137852283(C;G) on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.

SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.