rs4713586

A SNP on chromosome 6. Its most notable genotype is A;A: common in complete genomics

Gene
None listed
Location
Chr 632,691,805 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
8%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. A;AMost notableGoodcommon in complete genomicsTypical · 0.083% of people

SNPedia records rs4713586 on the minus strand: (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 83%
  • European ancestry (Utah)A;A 95%
  • Han Chinese (Beijing)A;A 82%
  • Japanese (Tokyo)A;A 76%
  • Yoruba (Nigeria)A;A 79%

Genosets

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

Notes

From SNPedia

Notes

rs4713586 is one of three HLA region SNPs used to tag the DQ2.2 haplotype in gs221.

Source and license

Adapted from rs4713586 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.