Variant: rs10498635 

    present in Gene: RIN3
    present in Chromosome: 14
    Position on Chromosome: 92636964
    Alleles of this Variant: C/T

rs10498635 in RIN3 gene and Osteitis Deformans PMID 21623375 2011 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.

PMID 20436471 2010 Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.

rs10498635 in RIN3 gene and Paget Disease PMID 20436471 2010 Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.

PMID 21623375 2011 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.

rs10498635 in RIN3 gene and response to bronchodilator PMID 26634245 2015 A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.