{{Rsnum
|rsid=2841498
|Chromosome=9
|position=85315130
|Orientation=plus
|GMAF=0.1331
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 2.7 | 27.4 | 69.9
| HCB | 0.7 | 10.9 | 88.3
| JPT | 1.8 | 17.7 | 80.5
| YRI | 0.0 | 4.1 | 95.9
| ASW | 0.0 | 8.8 | 91.2
| CHB | 0.7 | 10.9 | 88.3
| CHD | 0.9 | 11.1 | 88.0
| GIH | 1.0 | 21.8 | 77.2
| LWK | 0.0 | 3.7 | 96.3
| MEX | 8.6 | 34.5 | 56.9
| MKK | 0.0 | 11.5 | 88.5
| TSI | 1.0 | 24.5 | 74.5
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20522523
|Trait=Partial epilepsies
|Title=Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study
|RiskAllele=
|Pval=0.000004
|OR=None
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}