rs1038304

A SNP in the LOC107986528 gene on chromosome 6. Its most notable genotype is A;G.

Gene
LOC107986528
Location
Chr 6151,612,040 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
46%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;GMost notableNot ratedNo summary available.Typical · 0.040% of people

On SNPedia: (A;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;G 40%
  • European ancestry (Utah)A;G 55%
  • Han Chinese (Beijing)A;G 55%
  • Japanese (Tokyo)A;G 43%
  • Yoruba (Nigeria)A;G 17%
  • African ancestry (Southwest US)A;G 39%
  • Chinese (Denver)A;G 52%
  • Gujarati IndianA;G 52%
  • Luhya (Kenya)A;G 8%
  • Mexican ancestry (Los Angeles)A;G 38%
  • Maasai (Kenya)A;G 30%
  • TuscanA;G 47%

Other LOC107986528 SNPs

All LOC107986528 SNPs

Notes

From SNPedia

Notes

rs1038304 increases susceptibility to Bone mineral density variations, lower for carriers of the G allele

Source and license

Adapted from rs1038304 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.