{{Rsnum
|rsid=6904029
|Gene=MICD
|Chromosome=6
|position=29975290
|Orientation=plus
|GMAF=0.2842
|Gene_s=HCG9
|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 | 9.7 | 50.4 | 39.8
| HCB | 10.9 | 43.8 | 45.3
| JPT | 6.2 | 37.2 | 56.6
| YRI | 2.7 | 32.0 | 65.3
| ASW | 1.8 | 45.6 | 52.6
| CHB | 10.9 | 43.8 | 45.3
| CHD | 7.3 | 54.1 | 38.5
| GIH | 3.0 | 19.8 | 77.2
| LWK | 5.5 | 39.1 | 55.5
| MEX | 6.9 | 43.1 | 50.0
| MKK | 1.9 | 26.9 | 71.2
| TSI | 9.8 | 36.3 | 53.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20410501
|Trait=Vitiligo
|Title=Variant of TYR and Autoimmunity Susceptibility Loci in Generalized Vitiligo
|RiskAllele=A
|Pval=1E-21
|OR=1.49
|ORtxt=[1.37-1.61]
|OA=1
}}

{{omim
|id=193200
|rsnum=6904029
}}

{{PMID Auto
|PMID=22286212
|Title=Genome-Wide Association Study of Classical Hodgkin Lymphoma and Epstein-Barr Virus Status-Defined Subgroups
|OA=1
}}

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

{{GET Evidence
|gene=HCG9
|aa_change=Gly47Arg
|aa_change_short=G47R
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6904029
|overall_frequency_n=29
|overall_frequency_d=126
|overall_frequency=0.230159
|n_genomes=22
|n_genomes_annotated=0
|n_haplomes=24
|n_articles=0
|n_articles_annotated=0
|nblosum100=6
|autoscore=0
|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}}