rs2844682

A SNP on chromosome 6. Its most notable genotype is A;A.

Gene
None listed
Location
Chr 630,978,371 (GRCh38)
Highest magnitude
3.0Important
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
15%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;GGoodcommon in complete genomicsTypical · 0.076% of people
  2. A;AMost notableNot ratedNo summary available.Important · 3.02% of people

SNPedia records rs2844682 on the minus strand: (C;C), (T;T). 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.

  • AverageG;G 76% A;A 2%
  • European ancestry (Utah)G;G 79% A;A 0%
  • Han Chinese (Beijing)G;G 78% A;A <1%
  • Japanese (Tokyo)G;G 66% A;A 2%
  • Yoruba (Nigeria)G;G 77% A;A 3%
  • African ancestry (Southwest US)G;G 70% A;A 0%
  • Chinese (Denver)G;G 83% A;A 2%
  • Gujarati IndianG;G 87% A;A 1%
  • Luhya (Kenya)G;G 80% A;A 3%
  • Mexican ancestry (Los Angeles)G;G 59% A;A 5%
  • Maasai (Kenya)G;G 88% A;A 0%
  • TuscanG;G 68% A;A 1%

Genosets

Genosets combine several genotypes. Twofold checks them in your report.

Notes

From SNPedia

Notes

Helps to identify HLA-B*1502

Source and license

Adapted from rs2844682 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.