FMN2, formin 2, 56776

N. diseases: 88; N. variants: 27
Disease: Bone Density ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9287237
rs9287237
Entrez Id: 56776
Gene Symbol: FMN2
FMN2
CUI: C0005938
Disease:
Bone Density 		T 0.700 GeneticVariation GWASCAT Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure. 23437003 2013