rs5017717
A SNP in the PROS1 gene on chromosome 3. Its most notable genotype is G;G: common in clinvar
- Gene
- PROS1
- Location
- Chr 393,884,869 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs5017717 on the minus strand: (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.
- AverageG;G 100%
- European ancestry (Utah)G;G 100%
- Han Chinese (Beijing)G;G 100%
- Japanese (Tokyo)G;G 100%
- Yoruba (Nigeria)G;G 100%
Related
Other PROS1 SNPs
- rs387906675C;CProtein-S deficiency; severeVery important
- rs121918472G;GIncreased venous thromboembolism risk (> 6x)Very important
- rs138925964T;TClotting issues likely in infantsVery important
- rs6122A;GPartial protein-S deficiency; higher risk for blood clotting related issuesVery important
- rs121918473C;TPartial protein-S deficiency; higher risk for blood clotting related issuesVery important
- rs121918474C;TPartial protein-S deficiency; higher risk for blood clotting related issuesVery important
- rs121918475A;GPartial protein-S deficiency; higher risk for blood clotting related issuesVery important
- rs121918476C;GPartial protein-S deficiency; higher risk for blood clotting related issuesVery important
Source and license
Adapted from rs5017717 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.