rs1057911(A;T)
Carrier of one CYP2C9_50298A>T allele
- Magnitude
- 3.0Important
- Repute
- Not rated
- Frequency
- 7%Average of 4 populations
- On SNPedia
- rs1057911(A;T)
- Gene
- CYP2C9
Frequency
Share of people with A;T in each HapMap population.
- European ancestry (Utah)11%
- Han Chinese (Beijing)9%
- Japanese (Tokyo)7%
- Yoruba (Nigeria)0%
Other genotypes of rs1057911
Notes
From SNPedia
possibly influences Warfarin dosing
Related
Source and license
Adapted from rs1057911(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.