{{Rsnum
|rsid=10812428
|Chromosome=9
|position=26614849
|Orientation=plus
|GMAF=0.4073
|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 | 37.5 | 48.2 | 14.3
| HCB | 35.1 | 51.5 | 13.4
| JPT | 44.2 | 46.0 | 9.7
| YRI | 30.1 | 49.3 | 20.5
| ASW | 33.3 | 45.6 | 21.1
| CHB | 35.1 | 51.5 | 13.4
| CHD | 35.8 | 48.6 | 15.6
| GIH | 60.0 | 33.0 | 7.0
| LWK | 26.6 | 58.7 | 14.7
| MEX | 27.6 | 48.3 | 24.1
| MKK | 36.8 | 47.1 | 16.1
| TSI | 42.2 | 42.2 | 15.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19483685
|Trait=Drug-induced liver injury (flucloxacillin)
|Title=HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin
|RiskAllele=
|Pval=0.000001
|OR=2.85
|ORtxt=[NR]
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs10812428
|overall_frequency_n=53
|overall_frequency_d=124
|overall_frequency=0.427419
|n_genomes=36
|n_genomes_annotated=0
|n_haplomes=47
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}