rs396991, FCGR3A

N. diseases: 14
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Guillain-Barre Syndrome
CUI: C0018378
Disease: Guillain-Barre Syndrome
0.010 GeneticVariation BEFREE We assessed whether polymorphisms rs1801274 in FCGR2A and rs396991 in FCGR3A were associated with GBS in a Brazilian population. 27609290 2016