Variant: rs1561570

present in Gene: OPTN present in Chromosome: 10 Position on Chromosome: 13113726 Alleles of this Variant: T/C

rs1561570 in OPTN gene and Osteitis Deformans 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.

rs1561570 in OPTN 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.