rs2884737
A SNP in the VKORC1 gene on chromosome 16. Its most notable genotype is A;A: common in clinvar
- Gene
- VKORC1
- Location
- Chr 1631,094,233 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 13%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 8 HapMap populations.
- AverageA;A 79%
- European ancestry (Utah)A;A 58%
- Han Chinese (Beijing)A;A 99%
- African ancestry (Southwest US)A;A 91%
- Gujarati IndianA;A 86%
- Luhya (Kenya)A;A 97%
- Mexican ancestry (Los Angeles)A;A 76%
- Maasai (Kenya)A;A 80%
- TuscanA;A 43%
Related
Source and license
Adapted from rs2884737 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.