Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909149
rs121909149
SH3BP2
0.020 GeneticVariation BEFREE Therefore, we investigated whether P416R mutant SH3BP2 is involved in TNF-α-mediated osteoclast formation and bone loss. 24916406

2014
dbSNP: rs121909149
rs121909149
SH3BP2
0.020 GeneticVariation BEFREE A mouse model carrying a Pro416Arg mutation in SH3BP2 develops osteopenia and expansile lytic lesions in bone and some soft tissue organs. 22640988

2012