rs2001350

A SNP in the NFE2L2 gene on chromosome 2. Its most notable genotype is T;T: common in complete genomics

Gene
NFE2L2
Location
Chr 2177,235,697 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
15%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TMost notableGoodcommon in complete genomicsTypical · 0.072% of people

SNPedia records rs2001350 on the minus strand: (A;A). 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.

  • AverageT;T 72%
  • European ancestry (Utah)T;T 82%
  • Han Chinese (Beijing)T;T 53%
  • Japanese (Tokyo)T;T 62%
  • Yoruba (Nigeria)T;T 77%
  • African ancestry (Southwest US)T;T 81%
  • Chinese (Denver)T;T 57%
  • Gujarati IndianT;T 79%
  • Luhya (Kenya)T;T 76%
  • Mexican ancestry (Los Angeles)T;T 72%
  • Maasai (Kenya)T;T 67%
  • TuscanT;T 80%

Other NFE2L2 SNPs

All NFE2L2 SNPs

Source and license

Adapted from rs2001350 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.