{{Rsnum
|rsid=3823355
|Gene=HCG9
|Chromosome=6
|position=29974306
|Orientation=plus
|GMAF=0.2805
|Gene_s=HCG9
|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 | 39.8 | 50.4 | 9.7
| HCB | 45.6 | 43.4 | 11.0
| JPT | 57.5 | 36.3 | 6.2
| YRI | 64.6 | 32.7 | 2.7
| ASW | 52.6 | 45.6 | 1.8
| CHB | 45.6 | 43.4 | 11.0
| CHD | 39.3 | 53.3 | 7.5
| GIH | 77.2 | 19.8 | 3.0
| LWK | 55.5 | 39.1 | 5.5
| MEX | 50.9 | 42.1 | 7.0
| MKK | 71.4 | 26.6 | 1.9
| TSI | 52.9 | 37.3 | 9.8
| HapMapRevision=28
}}[[Generalized Vitiligo]]

{{PMID Auto
|PMID=19010793
|Title=Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.
}}

{{PMID Auto
|PMID=20593013
|Title=A major histocompatibility Class I locus contributes to multiple sclerosis susceptibility independently from HLA-DRB1*15:01.
|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}}