rs2515641
A SNP in the CYP2E1 gene on chromosome 10. Its most notable genotype is T;T: CYP2E1_10463T>C(F421F) homozygote
- Gene
- CYP2E1
- Location
- Chr 10133,537,858 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 27%
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CGoodnormal
- C;TNot ratedcarrier of one CYP2E1_10463T>C(F421F) allele
- T;TMost notableBadCYP2E1_10463T>C(F421F) homozygote
On SNPedia: (C;C), (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageC;C 49% C;T 35% T;T 16%
- European ancestry (Utah)C;C 74% C;T 26% T;T 0%
- Han Chinese (Beijing)C;C 65% C;T 34% T;T 2%
- Japanese (Tokyo)C;C 65% C;T 33% T;T 2%
- Yoruba (Nigeria)C;C 10% C;T 51% T;T 39%
- African ancestry (Southwest US)C;C 18% C;T 46% T;T 37%
- Chinese (Denver)C;C 77% C;T 23% T;T 0%
- Gujarati IndianC;C 71% C;T 27% T;T 2%
- Luhya (Kenya)C;C 5% C;T 41% T;T 55%
- Mexican ancestry (Los Angeles)C;C 69% C;T 24% T;T 7%
- Maasai (Kenya)C;C 14% C;T 52% T;T 34%
- TuscanC;C 69% C;T 31% T;T 0%
Related
Other CYP2E1 SNPs
- rs2070672G;GCYP2E1*7_-352A>G homozygoteWorth knowing
- rs2070676G;GCYP2E1*1B homozygoteWorth knowing
- rs915908G;Gcommon in complete genomicsTypical
- rs915909C;CnormalTypical
- rs2031920C;CnormalTypical
- rs2070673A;ACYP2E1*7_-333T>A homozygoteTypical
- rs3813865G;Gcommon in complete genomicsTypical
- rs3813867C;CCYP2E1_-1295G>C homozygoteTypical
Notes
From SNPedia
Notes
rs2515641 is a SNP in the CYP2E1 gene. The rs2515641(T) allele defines the CYP2E1_10463T>C(F421F) variant.
Source and license
Adapted from rs2515641 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.