rs7085387

A SNP in the LOC105378316 gene on chromosome 10. Its most notable genotype is A;G.

Gene
LOC105378316
Location
Chr 1058,444,842 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
38%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;GMost notableNot ratedNo summary available.Typical · 0.045% of people
  2. G;GNot ratedNo summary available.Typical · 0.021% of people

On SNPedia: (A;G), (G;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 45% G;G 21%
  • European ancestry (Utah)A;G 35% G;G 5%
  • Han Chinese (Beijing)A;G 45% G;G 12%
  • Japanese (Tokyo)A;G 54% G;G 18%
  • Yoruba (Nigeria)A;G 41% G;G 51%
  • African ancestry (Southwest US)A;G 44% G;G 44%
  • Chinese (Denver)A;G 56% G;G 3%
  • Gujarati IndianA;G 50% G;G 23%
  • Luhya (Kenya)A;G 38% G;G 39%
  • Mexican ancestry (Los Angeles)A;G 40% G;G 5%
  • Maasai (Kenya)A;G 50% G;G 25%
  • TuscanA;G 36% G;G 7%

Notes

From SNPedia

Notes

Rs7085387 is an A/G variant located on chromosome 10 and has been linked to migraines without aura

A;G

Rs7085387 is an A/G variant located on chromosome 10 and has been linked to migraines without aura

G;G

Rs7085387 is an A/G variant located on chromosome 10 and has been linked to migraines without aura

References

Source and license

Adapted from rs7085387 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.