Condition: Paget Disease


rs2458413 in DCSTAMP;DPYS 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.

rs4294134 in NUP205 gene and Paget Disease 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.

rs4941107 in PIGN 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.

rs5742915 in PML gene and Paget Disease PMID 21623375 2011 Genome-wide association identifies three new susceptibility loci 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.

rs5910578 in SLC25A43 gene and Paget Disease PMID 21623375 2011 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.