rs6711382

A SNP in the NEB gene on chromosome 2. Its most notable genotype is A;A: common in clinvar

Gene
NEB
Location
Chr 2151,674,563 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
26%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableGoodcommon in clinvarTypical · 0.013% of people
  2. G;GGoodcommon in complete genomicsTypical · 0.048% of people

On SNPedia: (A;A), (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 13% G;G 48%
  • European ancestry (Utah)A;A <1% G;G 81%
  • Han Chinese (Beijing)A;A 16% G;G 38%
  • Japanese (Tokyo)A;A 22% G;G 22%
  • Yoruba (Nigeria)A;A 15% G;G 30%
  • African ancestry (Southwest US)A;A 28% G;G 37%
  • Chinese (Denver)A;A 25% G;G 33%
  • Gujarati IndianA;A 11% G;G 53%
  • Luhya (Kenya)A;A 9% G;G 39%
  • Mexican ancestry (Los Angeles)A;A 0% G;G 83%
  • Maasai (Kenya)A;A 16% G;G 36%
  • TuscanA;A 1% G;G 82%

Other NEB SNPs

All NEB SNPs

Source and license

Adapted from rs6711382 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.