Variant: rs12660382 

    present in Gene: HCP5
    present in Chromosome: 6
    Position on Chromosome: 31475546
    Alleles of this Variant: C/T

rs12660382 in HCP5 gene and Diabetes Mellitus, Insulin-Dependent PMID 17632545 2007 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.

rs12660382 in HCP5 gene and Pemphigus Vulgaris PMID 22437316 2012 Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris.

rs12660382 in HCP5 gene and Rheumatoid Arthritis PMID 19503088 2009 REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis.