{{Rsnum
|rsid=17002253
|Chromosome=4
|position=76850192
|Orientation=plus
|GMAF=0.09229
|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 | 0.0 | 8.0 | 92.0
| HCB | 0.7 | 19.0 | 80.3
| JPT | 0.0 | 15.0 | 85.0
| YRI | 6.8 | 34.0 | 59.2
| ASW | 7.0 | 26.3 | 66.7
| CHB | 0.7 | 19.0 | 80.3
| CHD | 2.8 | 14.7 | 82.6
| GIH | 2.0 | 16.8 | 81.2
| LWK | 7.3 | 38.2 | 54.5
| MEX | 0.0 | 5.2 | 94.8
| MKK | 3.8 | 30.8 | 65.4
| TSI | 0.0 | 2.0 | 98.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22379998
|Trait=None
|Title=Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.
|RiskAllele=
|Pval=0.000007
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}