{{Rsnum
|rsid=2717068
|Chromosome=2
|position=57867738
|Orientation=minus
|GMAF=0.2916
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 27.7 | 58.5 | 13.8
| HCB | 42.2 | 53.3 | 4.4
| JPT | 53.3 | 37.8 | 8.9
| YRI | 98.4 | 1.6 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 42.2 | 53.3 | 4.4
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| 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=T
  |Pval=4E-7
  |OR=1.27
  |ORtxt=[1.16-1.40]
  }}