FMN2, formin 2, 56776

N. diseases: 88; N. variants: 27
Disease: Serum HDL cholesterol measurement ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1456649
rs1456649
Entrez Id: 56776
Gene Symbol: FMN2
FMN2
CUI: C0428472
Disease:
Serum HDL cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012