{{Rsnum
|rsid=9268645
|Gene=HLA-DRA
|Chromosome=6
|position=32440750
|Orientation=plus
|GMAF=0.4091
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=HLA-DRA
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 34.5 | 51.3 | 14.2
| HCB | 21.2 | 40.9 | 38.0
| JPT | 38.1 | 46.9 | 15.0
| YRI | 40.8 | 49.7 | 9.5
| ASW | 50.9 | 36.8 | 12.3
| CHB | 21.2 | 40.9 | 38.0
| CHD | 10.1 | 56.9 | 33.0
| GIH | 33.7 | 40.6 | 25.7
| LWK | 57.8 | 33.0 | 9.2
| MEX | 27.6 | 58.6 | 13.8
| MKK | 44.9 | 44.9 | 10.3
| TSI | 24.5 | 58.8 | 16.7
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19430480
|Trait=Type 1 diabetes
|Title=Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes
|RiskAllele=
|Pval=1E-100
|OR=NR
|ORtxt=NR
|OA=1
}}

{{PMID|17660530}} Risk alleles for multiple sclerosis identified by a genomewide study.

{{PMID|20018019|OA=1
}} Two-stage joint selection method to identify candidate markers from genome-wide association studies.

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs9268645
|overall_frequency_n=50
|overall_frequency_d=128
|overall_frequency=0.390625
|n_genomes=31
|n_genomes_annotated=0
|n_haplomes=42
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}