Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs573658040
rs573658040
APOE
0.020 GeneticVariation BEFREE This analysis revealed an apoE2/E2 (arginine 145 to cysteine) mutation, previously reported to be a rare cause of type III HLP in 5 patients of African descent. 16690468

2006
dbSNP: rs573658040
rs573658040
APOE
0.020 GeneticVariation BEFREE We propose that in the analysed family this rare apo E2 (Arg-136-->Cys) variant is associated with late-onset dominance of type III HLP. 8682150

1996