{{Rsnum
|rsid=4646976
|Gene=CYP2E1
|Chromosome=10
|position=135347727
|Orientation=plus
|GMAF=0.08173
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 95.6 | 4.4 | 0.0
| HCB | 64.2 | 35.0 | 0.7
| JPT | 64.6 | 33.6 | 1.8
| YRI | 82.3 | 17.7 | 0.0
| ASW | 93.0 | 7.0 | 0.0
| CHB | 64.2 | 35.0 | 0.7
| CHD | 77.1 | 22.9 | 0.0
| GIH | 93.1 | 5.9 | 1.0
| LWK | 88.2 | 11.8 | 0.0
| MEX | 84.5 | 15.5 | 0.0
| MKK | 90.4 | 9.0 | 0.6
| TSI | 97.1 | 2.9 | 0.0
| HapMapRevision=28
}}[[rs4646976]] is a SNP in the [[CYP2E1]] gene.

The [[rs4646976]](G) allele defines the CYP2E1_marker8 variant, as used in the 2008 study determining the 16 most common CYP2E1 haplotypes world-wide.(see [[CYP2E1]] for details)

{{PMID Auto
|PMID=18663376
|Title=Global patterns of variation in allele and haplotype frequencies and linkage disequilibrium across the CYP2E1 gene.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}