rs6048
A SNP in the F9 gene on chromosome X. Its most notable genotype is A;G: slightly lower risk (10-20%) of deep vein thrombosis
- Gene
- F9
- Location
- Chr X139,551,121 (GRCh38)
- Highest magnitude
- 1.2Minor
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 16%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AGoodcommon
- A;GMost notableGoodslightly lower risk (10-20%) of deep vein thrombosis
- G;GGoodslightly lower risk (10-20%) of deep vein thrombosis
On SNPedia: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 5 HapMap populations.
- AverageA;A 88% A;G 6% G;G 6%
- European ancestry (Utah)A;A 55% A;G 19% G;G 26%
- Han Chinese (Beijing)A;A 100% A;G 0% G;G 0%
- Japanese (Tokyo)A;A 100% A;G 0% G;G 0%
- Yoruba (Nigeria)A;A 90% A;G 6% G;G 5%
- Luhya (Kenya)A;A 93% A;G 6% G;G <1%
Related
Conditions, medicines and genes
Other F9 SNPs
- i5007022A;G“royal disease” also known as hemophilia B or Christmas diseaseVery important
- rs398122990A;G“royal disease” also known as hemophilia B or Christmas diseaseVery important
- rs137852229C;CHemophilia B (severity varies)Very important
- rs137852230G;GHemophilia B (severity varies)Very important
- rs137852231C;CHemophilia B (severity varies)Very important
- rs137852232G;GHemophilia B (severity varies)Very important
- rs137852233A;AHemophilia B (severity varies)Very important
- rs137852234G;GHemophilia B (severity varies)Very important
Genosets
Genosets combine several genotypes. Twofold checks them in your report.
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 rs6048 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.