{{Rsnum
|rsid=602875
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Orientation=plus
|Chromosome=6
|position=32502100
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 77.9 | 19.5 | 2.7
| HCB | 42.2 | 40.0 | 17.8
| JPT | 35.4 | 51.3 | 13.3
| YRI | 41.5 | 44.2 | 14.3
| ASW | 54.4 | 35.1 | 10.5
| CHB | 42.2 | 40.0 | 17.8
| CHD | 39.4 | 46.8 | 13.8
| GIH | 84.0 | 14.0 | 2.0
| LWK | 33.9 | 45.9 | 20.2
| MEX | 43.1 | 48.3 | 8.6
| MKK | 50.0 | 43.6 | 6.4
| TSI | 43.1 | 50.0 | 6.9
| HapMapRevision=28
}}Variant in an [[HLA]] region is associated with lower susceptibility to [[leprosy]] in Asians, according to the [http://blog.23andme.com/2009/12/16/snpwatch-genetic-association-study-of-leprosy-yields-new-insights-into-an-ancient-disease/ 23andMe blog]. The protective allele is G, and the odds ratio is 0.67.

{{PMID Auto GWAS
|PMID=20018961
|Trait=Leprosy
|Title=Genomewide Association Study of Leprosy
|RiskAllele=A
|Pval=5E-27
|OR=1.61
|ORtxt=[1.39-1.61]
}}

{{PMID|20017974|OA=1
}} Simultaneous analysis of all single-nucleotide polymorphisms in genome-wide association study of rheumatoid arthritis.

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs602875
|overall_frequency_n=13
|overall_frequency_d=82
|overall_frequency=0.158537
|n_genomes=12
|n_genomes_annotated=0
|n_haplomes=13
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}