Variant: rs4941107

present in Gene: PIGN present in Chromosome: 18 Position on Chromosome: 62084098 Alleles of this Variant: A/G

rs4941107 in PIGN 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.

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.