rs3733403
A SNP in the F11 gene on chromosome 4. Its most notable genotype is C;C: common in clinvar
- Gene
- F11
- Location
- Chr 4186,265,981 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, FamilyTreeDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageC;C 58%
- European ancestry (Utah)C;C 76%
- Han Chinese (Beijing)C;C 49%
- Japanese (Tokyo)C;C 64%
- Yoruba (Nigeria)C;C 44%
Related
Other F11 SNPs
- rs28934608T;TFactor XI deficiencyVery important
- rs121965063T;TFactor XI deficiencyVery important
- rs121965064C;CFactor XI deficiencyVery important
- rs121965066A;AFactor XI deficiencyVery important
- rs121965067A;AFactor XI deficiencyVery important
- rs121965068T;TFactor XI deficiencyVery important
- rs121965069C;CFactor XI deficiencyVery important
- rs121965071T;TFactor XI deficiencyVery important
Source and license
Adapted from rs3733403 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.