rs2070672
A SNP in the CYP2E1 gene on chromosome 10. Its most notable genotype is G;G: CYP2E1*7_-352A>G homozygote
- Gene
- CYP2E1
- Location
- Chr 10133,527,044 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 12%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AGoodnormal
- A;GNot ratedcarrier of one CYP2E1*7_-352A>G allele
- G;GMost notableBadCYP2E1*7_-352A>G homozygote
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 11 HapMap populations.
- AverageA;A 74% A;G 24% G;G 2%
- European ancestry (Utah)A;A 93% A;G 7% G;G 0%
- Han Chinese (Beijing)A;A 62% A;G 33% G;G 5%
- Japanese (Tokyo)A;A 54% A;G 43% G;G 4%
- Yoruba (Nigeria)A;A 74% A;G 24% G;G 3%
- African ancestry (Southwest US)A;A 79% A;G 21% G;G 0%
- Chinese (Denver)A;A 69% A;G 31% G;G 0%
- Gujarati IndianA;A 52% A;G 41% G;G 8%
- Luhya (Kenya)A;A 81% A;G 16% G;G 3%
- Mexican ancestry (Los Angeles)A;A 83% A;G 17% G;G 0%
- Maasai (Kenya)A;A 75% A;G 24% G;G 1%
- TuscanA;A 93% A;G 7% G;G 0%
Related
Other CYP2E1 SNPs
- 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
- rs3813865G;Gcommon in complete genomicsTypical
- rs3813867C;CCYP2E1_-1295G>C homozygoteTypical
Notes
From SNPedia
Notes
rs2070672 is a SNP in the CYP2E1 gene. The rs2070672(G) allele defines the CYP2E1*7_-352A>G variant.
Source and license
Adapted from rs2070672 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.