{{Rsnum
|rsid=13026414
|Chromosome=2
|position=57706920
|Orientation=plus
|GMAF=0.2612
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LOC101927235
|Gene_s=LOC101927235
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 38.1 | 54.0 | 8.0
| HCB | 54.1 | 37.8 | 8.1
| JPT | 69.0 | 28.3 | 2.7
| YRI | 97.3 | 2.7 | 0.0
| ASW | 86.0 | 14.0 | 0.0
| CHB | 54.1 | 37.8 | 8.1
| CHD | 67.0 | 28.4 | 4.6
| GIH | 54.5 | 38.6 | 6.9
| LWK | 94.5 | 4.5 | 0.9
| MEX | 48.3 | 41.4 | 10.3
| MKK | 62.8 | 29.5 | 7.7
| TSI | 33.3 | 45.1 | 21.6
| 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=2E-9
  |OR=1.23
  |ORtxt=[1.15-1.32]
  }}

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