Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs573658040
rs573658040
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III
0.100 GeneticVariation BEFREE In an initiated study of Qataris, we observed that 17% of the African-derived genetic subgroup were heterozygotes for a rare Arg145Cys (R145C) variant that functions as a dominant trait with incomplete penetrance associated with type III hyperlipoproteinemia. 24239320

2014

dbSNP: rs573658040
rs573658040
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III
0.100 GeneticVariation BEFREE This finding supports the notion that although apoE 2*(Arg136-->Cys) mutation is perhaps not sufficient to cause FD itself, the presence of other genetic and/or environmental factors can lead to the phenotypic expression of the disease in the carriers. 14535841

2003

dbSNP: rs573658040
rs573658040
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III
0.100 GeneticVariation BEFREE We described the mutation apo E2* (Arg136 --> Cys) in a family with elevated lipid levels, but there was no confirmation of the connection between this mutation and type III hyperlipoproteinemia or hyperlipoproteinemia at all. 11043917

2000

dbSNP: rs573658040
rs573658040
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III
0.100 GeneticVariation BEFREE As the dominant apoE variants known so far are characterized by more pronounced reductions of heparin binding, we suggest that apoE2 (Arg136 --> Cys) is not associated with dominant expression of type III hyperlipoproteinemia. 9548597

1998

dbSNP: rs573658040
rs573658040
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III
0.100 GeneticVariation BEFREE The apolipoprotein E2 (Arg145Cys) mutation causes autosomal dominant type III hyperlipoproteinemia with incomplete penetrance. 9157949

1997

dbSNP: rs573658040
rs573658040
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III
0.100 GeneticVariation BEFREE Apolipoprotein E2 (Arg-136-->Cys), a variant of apolipoprotein E associated with late-onset dominance of type III hyperlipoproteinaemia. 8682150

1996

dbSNP: rs573658040
rs573658040
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III
0.100 GeneticVariation BEFREE Restriction isotyping of apolipoprotein E R145C in type III hyperlipoproteinemia. 7735921

1995

dbSNP: rs573658040
rs573658040
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III
0.100 GeneticVariation BEFREE In comparison, beta-VLDL+apoE(Arg142-->Cys), beta-VLDL+apoE(Arg145-->Cys), and beta-VLDL+apoE-Leiden, which are associated with dominant type III hyperlipoproteinemia, bound more poorly. 8175773

1994

dbSNP: rs573658040
rs573658040
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III
0.100 GeneticVariation BEFREE Heterozygosity for apolipoprotein E-4Philadelphia(Glu13----Lys, Arg145----Cys) is associated with incomplete dominance of type III hyperlipoproteinemia. 1352296

1992

dbSNP: rs573658040
rs573658040
CUI: C0020479
Disease: Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type III
0.100 GeneticVariation BEFREE Apolipoprotein E-4Philadelphia (Glu13----Lys,Arg145----Cys). Homozygosity for two rare point mutations in the apolipoprotein E gene combined with severe type III hyperlipoproteinemia. 1674745

1991

dbSNP: rs573658040
rs573658040
Hyperkeratosis lenticularis perstans
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
Hyperkeratosis lenticularis perstans
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

dbSNP: rs573658040
rs573658040
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias
0.010 GeneticVariation BEFREE Prevalence of the apolipoprotein E Arg145Cys dyslipidemia at-risk polymorphism in African-derived populations. 24239320

2014

dbSNP: rs573658040
rs573658040
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 GeneticVariation BEFREE Apolipoprotein E Arg136 --> Cys in individuals with premature myocardial infarction. 19545491

2009

dbSNP: rs573658040
rs573658040
CUI: C0302164
Disease: Tuberous xanthoma
Tuberous xanthoma
0.010 GeneticVariation BEFREE To our knowledge, this is the first report of an association between olanzapine therapy and tuberous xanthomas and the sixth report of this rare apoE2/E2 (arginine 145 to cysteine) mutation in the literature. 16690468

2006

dbSNP: rs573658040
rs573658040
CUI: C0020476
Disease: Hyperlipoproteinemias
Hyperlipoproteinemias
0.010 GeneticVariation BEFREE We described the mutation apo E2* (Arg136 --> Cys) in a family with elevated lipid levels, but there was no confirmation of the connection between this mutation and type III hyperlipoproteinemia or hyperlipoproteinemia at all. 11043917

2000

dbSNP: rs573658040
rs573658040
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.010 GeneticVariation BEFREE Variable expression of hypercholesterolemia in Apolipoprotein E2* (Arg136 --> Cys) heterozygotes. 11043917

2000

dbSNP: rs573658040
rs573658040
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.010 GeneticVariation BEFREE Two of the four apoE2 (Arg136 --> Cys)/3 heterozygotes had elevated triglycerides, two were normolipidemic. 9548597

1998

dbSNP: rs573658040
rs573658040
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia
0.010 GeneticVariation BEFREE Digestion with BbvI or Fnu4HI allows for rapid restriction isotyping for the rare apolipoprotein E R145C mutation associated with hyperlipidemia. 7735921

1995