rs4524
A SNP in the F5 gene on chromosome 1. Its most notable genotype is T;T: common in clinvar
- Gene
- F5
- Location
- Chr 1169,542,517 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 24%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs4524 on the minus strand: (A;A). 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 56%
- European ancestry (Utah)T;T 55%
- Han Chinese (Beijing)T;T 66%
- Japanese (Tokyo)T;T 63%
- Yoruba (Nigeria)T;T 69%
- African ancestry (Southwest US)T;T 53%
- Chinese (Denver)T;T 60%
- Gujarati IndianT;T 37%
- Luhya (Kenya)T;T 66%
- Mexican ancestry (Los Angeles)T;T 41%
- Maasai (Kenya)T;T 53%
- TuscanT;T 58%
Related
Conditions, medicines and genes
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
Gene variants associated with deep vein thrombosis. Updated analysis of gene variants associated with deep vein thrombosis.
Source and license
Adapted from rs4524 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.