Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12713559
rs12713559
APOB
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.010 GeneticVariation BEFREE The Arg3531-->Cys mutation is the second reported cause of familial ligand-defective apoB. 7883971

1995