rs6413419
A SNP in the CYP2E1 gene on chromosome 10. Its most notable genotype is A;A: CYP2E1*4 homozygote
- Gene
- CYP2E1
- Location
- Chr 10133,532,171 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 7%
Genotypes
As shown in 23andMe and AncestryDNA files.
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 10 HapMap populations.
- AverageA;A 1% A;G 15% G;G 84%
- European ancestry (Utah)A;A 0% A;G 4% G;G 96%
- Han Chinese (Beijing)A;A 0% A;G 0% G;G 100%
- Japanese (Tokyo)A;A 0% A;G 0% G;G 100%
- Yoruba (Nigeria)A;A 8% A;G 44% G;G 48%
- African ancestry (Southwest US)A;A 4% A;G 39% G;G 58%
- Gujarati IndianA;A 0% A;G 2% G;G 98%
- Luhya (Kenya)A;A <1% A;G 29% G;G 70%
- Mexican ancestry (Los Angeles)A;A 0% A;G 9% G;G 91%
- Maasai (Kenya)A;A 0% A;G 16% G;G 84%
- TuscanA;A 0% A;G 8% G;G 92%
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
- rs3813865G;Gcommon in complete genomicsTypical
Notes
From SNPedia
Notes
rs6413419, also known as 4768G>A or V179I, is a SNP in the CYP2E1 gene. The rs6413419(A) allele defines the CYP2E1*4 variant.
Source and license
Adapted from rs6413419 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.