rs3813865
A SNP in the CYP2E1 gene on chromosome 10. Its most notable genotype is G;G: common in complete genomics
- Gene
- CYP2E1
- Location
- Chr 10133,525,740 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 12%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (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.
- AverageG;G 71%
- European ancestry (Utah)G;G 95%
- Han Chinese (Beijing)G;G 64%
- Japanese (Tokyo)G;G 55%
- Yoruba (Nigeria)G;G 70%
Related
Other CYP2E1 SNPs
- rs2070672G;GCYP2E1*7_-352A>G homozygoteWorth knowing
- rs2070676G;GCYP2E1*1B homozygoteWorth knowing
- rs2515641T;TCYP2E1_10463T>C(F421F) homozygoteWorth knowing
- rs915908G;Gcommon in complete genomicsTypical
- rs915909C;CnormalTypical
- rs2031920C;CnormalTypical
- rs2070673A;ACYP2E1*7_-333T>A homozygoteTypical
- rs3813867C;CCYP2E1_-1295G>C homozygoteTypical
Source and license
Adapted from rs3813865 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.