rs5988
A SNP in the F13A1 gene on chromosome 6. Its most notable genotype is C;C: common in clinvar
- Gene
- F13A1
- Location
- Chr 66,151,904 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 19%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs5988 on the minus strand: (G;G). 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 69%
- European ancestry (Utah)C;C 55%
- Han Chinese (Beijing)C;C 84%
- Japanese (Tokyo)C;C 82%
- Yoruba (Nigeria)C;C 54%
Related
Notes
From SNPedia
Notes
Common hemostasis and inflammation gene variants and venous thrombosis in older adults from the Cardiovascular Health Study.
Source and license
Adapted from rs5988 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.