rs3823355

This variant is located in the HCG9 gene.

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GWAS Catalog Trait Associations (1)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

Vitiligo

Jin Y et al. “Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo.” The New England Journal of Medicine 362(18):1686-97 (2010)

Allele T

OR 1.50

p 9.0e-23

N 4,021

Large GWAS

European

About HCG9

This gene lies within the MHC class I region on chromosome 6p21.3. This gene is believed to be non-coding, but its function has not been determined. [provided by RefSeq, Jul 2009]

View all HCG9 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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