rs1834640

A SNP on chromosome 15. Its most notable genotype is A;A: common in complete genomics

Gene
None listed
Location
Chr 1548,099,968 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
49%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableGoodcommon in complete genomicsTypical · 0.031% of people

On SNPedia: (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.

  • AverageA;A 31%
  • European ancestry (Utah)A;A 98%
  • Han Chinese (Beijing)A;A 2%
  • Japanese (Tokyo)A;A 0%
  • Yoruba (Nigeria)A;A 0%
  • African ancestry (Southwest US)A;A 0%
  • Chinese (Denver)A;A 0%
  • Gujarati IndianA;A 88%
  • Luhya (Kenya)A;A <1%
  • Mexican ancestry (Los Angeles)A;A 47%
  • Maasai (Kenya)A;A 9%
  • TuscanA;A 99%

Notes

From SNPedia

Notes

Genome-wide association study SNPs in the human genome diversity project populations: does selection affect unlinked SNPs with shared trait associations?

Source and license

Adapted from rs1834640 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.