{{Rsnum
|rsid=7798500
|Chromosome=7
|position=107021638
|Orientation=plus
|GMAF=0.1382
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 91.2 | 8.8 | 0.0
| HCB | 86.7 | 13.3 | 0.0
| JPT | 95.6 | 4.4 | 0.0
| YRI | 28.8 | 48.6 | 22.6
| ASW | 43.9 | 40.4 | 15.8
| CHB | 86.7 | 13.3 | 0.0
| CHD | 88.1 | 11.0 | 0.9
| GIH | 94.1 | 5.9 | 0.0
| LWK | 29.0 | 53.3 | 17.8
| MEX | 94.8 | 5.2 | 0.0
| MKK | 38.7 | 48.4 | 12.9
| TSI | 96.1 | 3.9 | 0.0
| 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=0.000006
|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}}