rs4525
A SNP in the F5 gene on chromosome 1. Its most notable genotype is T;T: common in clinvar
- Gene
- F5
- Location
- Chr 1169,542,496 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 24%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- T;TMost notableGoodcommon in clinvar
- C;TNot ratedNo summary available.
- C;CNot ratedNo summary available.
SNPedia records rs4525 on the minus strand: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageT;T 57% C;T 37% C;C 6%
- European ancestry (Utah)T;T 55% C;T 38% C;C 7%
- Han Chinese (Beijing)T;T 67% C;T 31% C;C 2%
- Japanese (Tokyo)T;T 64% C;T 32% C;C 4%
- Yoruba (Nigeria)T;T 69% C;T 30% C;C 2%
- African ancestry (Southwest US)T;T 53% C;T 40% C;C 7%
- Chinese (Denver)T;T 59% C;T 36% C;C 5%
- Gujarati IndianT;T 39% C;T 55% C;C 7%
- Luhya (Kenya)T;T 66% C;T 32% C;C 2%
- Mexican ancestry (Los Angeles)T;T 41% C;T 35% C;C 24%
- Maasai (Kenya)T;T 53% C;T 42% C;C 5%
- TuscanT;T 58% C;T 36% C;C 6%
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
Source and license
Adapted from rs4525 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.