{{Rsnum
|rsid=11966200
|Gene=SLC44A4
|Chromosome=6
|position=31869289
|Orientation=plus
|GMAF=0.04591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SLC44A4
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 96.5 | 3.5 | 0.0
| HCB | 92.0 | 8.0 | 0.0
| JPT | 98.2 | 1.8 | 0.0
| YRI | 81.0 | 19.0 | 0.0
| ASW | 73.7 | 26.3 | 0.0
| CHB | 92.0 | 8.0 | 0.0
| CHD | 94.5 | 5.5 | 0.0
| GIH | 98.0 | 2.0 | 0.0
| LWK | 79.1 | 20.0 | 0.9
| MEX | 91.4 | 8.6 | 0.0
| MKK | 80.1 | 19.2 | 0.6
| TSI | 91.2 | 8.8 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20526339
|Trait=Vitiligo
|Title=Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC
|RiskAllele=A
|Pval=1E-48
|OR=1.90
|ORtxt=[1.74-2.07]
}}

{{omim
|id=193200
|rsnum=11966200
}}

{{PMID Auto
|PMID=23516070
|Title=The association between a single nucleotide polymorphism rs11966200 in MHC region and clinical features of generalized vitiligo in Chinese Han population
}}

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