rs7742369

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

Gene
None listed
Location
Chr 634,197,944 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
30%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableGoodcommon in complete genomicsTypical · 0.047% 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 47%
  • European ancestry (Utah)A;A 70%
  • Han Chinese (Beijing)A;A 77%
  • Japanese (Tokyo)A;A 68%
  • Yoruba (Nigeria)A;A 16%
  • African ancestry (Southwest US)A;A 16%
  • Chinese (Denver)A;A 75%
  • Gujarati IndianA;A 71%
  • Luhya (Kenya)A;A 14%
  • Mexican ancestry (Los Angeles)A;A 19%
  • Maasai (Kenya)A;A 31%
  • TuscanA;A 65%

Notes

From SNPedia

Notes

Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.

Source and license

Adapted from rs7742369 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.