FAP, fibroblast activation protein alpha, 2191

N. diseases: 216; N. variants: 7
Disease: Familial (FPAH) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs946880677
rs946880677
Entrez Id: 2191
Gene Symbol: FAP
FAP
CUI: C1611743
Disease:
Familial (FPAH) 		0.010 GeneticVariation BEFREE To clarify the pathogenesis of leptomeningeal amyloidosis in familial amyloidotic polyneuropathy amyloidogenic transthyretin Y114C (FAP ATTR Y114C). 16217058 2005