rs121965065
A SNP in the F11-AS1 gene on chromosome 4. Its most notable genotype is G;G: Factor XI deficiency
- Gene
- F11-AS1
- Location
- Chr 4186,285,711 (GRCh38)
- Highest magnitude
- 5.0Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- G;GMost notableBadFactor XI deficiency
- G;TBadcarrier of factor XI mutation
- T;TGoodcommon in clinvar
On SNPedia: (G;G), (G;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
aka c.1378T>G (p.Phe460Val) 23andMe name: i5001640
G;T
Usually not affected in absence of a second F11 gene mutation
Source and license
Adapted from rs121965065 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.