rs2228152(A;T)

Carrier of a Hemophilia A mutation

Magnitude
3.5Important
Repute
Bad
Frequency
0%Average of 1 populations
On SNPedia
rs2228152(A;T)Minus strand
Gene
F8

Frequency

Share of people with A;T in each HapMap population.

  • European ancestry (Utah)0%

Other genotypes of rs2228152

  1. T;TGoodcommon in clinvarTypical · 0.0100% of people
  2. A;AMost notableBadHemophilia A (severity varies)Very important · 5.50% of people

All about rs2228152

Notes

From SNPedia

X-linked recessive, so females are generally unaffected in the absence of a second F8 gene mutation, however some females may experience clotting issues.

Source and license

Adapted from rs2228152(A;T) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.