{{Rsnum
|rsid=771390
|Chromosome=1
|position=34285335
|Orientation=plus
|GMAF=0.1648
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 73.5 | 18.6 | 8.0
| HCB | 80.3 | 19.0 | 0.7
| JPT | 74.1 | 23.2 | 2.7
| YRI | 73.5 | 23.8 | 2.7
| ASW | 75.4 | 22.8 | 1.8
| CHB | 80.3 | 19.0 | 0.7
| CHD | 77.8 | 21.3 | 0.9
| GIH | 79.2 | 17.8 | 3.0
| LWK | 67.3 | 30.9 | 1.8
| MEX | 64.9 | 31.6 | 3.5
| MKK | 74.4 | 25.0 | 0.6
| TSI | 53.9 | 40.2 | 5.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22949513
  |Trait=Epilepsy (generalized)
  |Title=Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32
  |RiskAllele=C
  |Pval=6E-7
  |OR=1.22
  |ORtxt=[1.12-1.32]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}