rs118203912
A SNP in the F5 gene on chromosome 1. Its most notable genotype is A;A: Hemophilia A (severity varies)
- Gene
- F5
- Location
- Chr 1169,560,701 (GRCh38)
- Highest magnitude
- 5.5Very important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- C;CGoodcommon in clinvar
- A;CBadThrombophilia risk
- A;AMost notableBadHemophilia A (severity varies)
SNPedia records rs118203912 on the minus strand: (G;G), (G;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other F5 SNPs
- rs6025T;T11.4x higher risk of thrombosisVery important
- rs118203905C;CHemophilia A (severity varies)Very important
- rs118203906G;GHemophilia A (severity varies)Very important
- rs118203907C;CHemophilia A (severity varies)Very important
- rs118203908A;AHemophilia A (severity varies)Very important
- rs118203909A;AHemophilia A (severity varies)Very important
- rs118203910A;AHemophilia A (severity varies)Very important
- rs118203911G;GHemophilia A (severity varies)Very important
Notes
From SNPedia
Notes
A;C
May have higher thrombophilia risk due to activated protein C resistance; see ClinVar & OMIM
Source and license
Adapted from rs118203912 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.