rs3819102
A SNP in the ENOSF1 gene on chromosome 18. Its most notable genotype is A;A: common in complete genomics
- Gene
- ENOSF1
- Location
- Chr 18675,307 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- 9%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs3819102 on the minus strand: (T;T). 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.
- AverageA;A 79%
- European ancestry (Utah)A;A 95%
- Han Chinese (Beijing)A;A 60%
- Japanese (Tokyo)A;A 64%
- Yoruba (Nigeria)A;A 95%
Notes
From SNPedia
Notes
rs3819102 associated with risk of endometrial cancer. The odds ratio (95% confidence interval) for the CC genotype was 1.5 (1.0-2.2) compared with the TT genotype
Source and license
Adapted from rs3819102 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.