rs2070673

A SNP in the CYP2E1 gene on chromosome 10. Its most notable genotype is A;A: CYP2E1*7_-333T>A homozygote

Gene
CYP2E1
Location
Chr 10133,527,063 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
40%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableNot ratedCYP2E1*7_-333T>A homozygoteTypical · 0.031% of people
  2. A;TNot ratedcarrier of one CYP2E1*7_-333T>A alleleTypical · 0.036% of people
  3. T;TGoodnormalTypical · 0.033% of people

On SNPedia: (A;A), (A;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 4 HapMap populations.

  • AverageA;A 31% A;T 36% T;T 33%
  • European ancestry (Utah)A;A 2% A;T 29% T;T 69%
  • Han Chinese (Beijing)A;A 24% A;T 44% T;T 31%
  • Japanese (Tokyo)A;A 22% A;T 46% T;T 32%
  • Yoruba (Nigeria)A;A 74% A;T 24% T;T 2%

Notes

From SNPedia

Notes

rs2070673 is a SNP in the CYP2E1 gene. The rs2070673(A) allele defines the CYP2E1*7_-333T>A variant.

Source and license

Adapted from rs2070673 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.