Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1801274
rs1801274
Entrez Id: 2212
Gene Symbol: FCGR2A
FCGR2A
CUI: C0010346
Disease:
Crohn Disease
A 0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919 2015