{{Rsnum
|rsid=2844665
|Chromosome=6
|position=31039078
|Orientation=minus
|GMAF=0.3843
|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 | 15.0 | 48.7 | 36.3
| HCB | 20.4 | 50.4 | 29.2
| JPT | 14.2 | 56.6 | 29.2
| YRI | 10.2 | 43.5 | 46.3
| ASW | 14.0 | 40.4 | 45.6
| CHB | 20.4 | 50.4 | 29.2
| CHD | 31.2 | 47.7 | 21.1
| GIH | 8.9 | 33.7 | 57.4
| LWK | 10.9 | 35.5 | 53.6
| MEX | 13.8 | 36.2 | 50.0
| MKK | 14.2 | 41.3 | 44.5
| TSI | 9.8 | 49.0 | 41.2
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21801394
|Trait=None
|Title=Genome-Wide Association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe.
|RiskAllele=C
|Pval=3E-7
|OR=1.5400
|ORtxt=[1.30-1.82]
|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}}