Gene: FCGRT ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2217
Gene Symbol: FCGRT
FCGRT 		0.020 GeneticVariation disease BEFREE Afibrinogenemia resulting from homozygous nonsense mutation in A alpha chain gene associated with multiple thrombotic episodes. 18388508 2008
Entrez Id: 2217
Gene Symbol: FCGRT
FCGRT 		0.020 GeneticVariation disease BEFREE A case of afibrinogenemia associated with A-alpha chain gene compound heterozygosity (HUMFIBRA c.[4110delA]+[3200+1G>T]). 17179831 2007