{{Rsnum
|rsid=7085387
|Chromosome=10
|position=60204602
|Orientation=plus
|GMAF=0.3792
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 59.3 | 35.4 | 5.3
| HCB | 42.3 | 45.3 | 12.4
| JPT | 28.3 | 54.0 | 17.7
| YRI | 7.6 | 41.0 | 51.4
| ASW | 12.3 | 43.9 | 43.9
| CHB | 42.3 | 45.3 | 12.4
| CHD | 41.3 | 56.0 | 2.8
| GIH | 27.7 | 49.5 | 22.8
| LWK | 22.7 | 38.2 | 39.1
| MEX | 55.2 | 39.7 | 5.2
| MKK | 24.5 | 50.3 | 25.2
| TSI | 56.9 | 36.3 | 6.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23793025
  |Trait=Migraine without aura
  |Title=Genome-wide meta-analysis identifies new susceptibility loci for migraine.
  |RiskAllele=
  |Pval=2E-6
  |OR=1.14
  |ORtxt=[1.08-1.19]
  }}

Rs7085387 is an A/G variant located on chromosome 10 and has been linked to migraines without aura {{PMID|23793025}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}