Variant: rs725613 

    present in Gene: CLEC16A
    present in Chromosome: 16
    Position on Chromosome: 11075826
    Alleles of this Variant: T/G

rs725613 in CLEC16A gene and Cholangitis, Sclerosing PMID 27992413 2017 Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease.

rs725613 in CLEC16A gene and Diabetes Mellitus, Insulin-Dependent PMID 17632545 2007 Three common non-coding variants of the gene (rs2903692, rs725613 and rs17673553) in strong linkage disequilibrium reached genome-wide significance for association with T1D.

rs725613 in CLEC16A gene and Primary biliary cirrhosis PMID 21399635 2011 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.