Gene: APOE ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs769452
rs769452
APOE
0.700 GeneticVariation UNIPROT Global molecular analysis and APOE mutations in a cohort of autosomal dominant hypercholesterolemia patients in France. 26802169

2016
dbSNP: rs769455
rs769455
APOE
0.700 GeneticVariation UNIPROT Global molecular analysis and APOE mutations in a cohort of autosomal dominant hypercholesterolemia patients in France. 26802169

2016
dbSNP: rs769452
rs769452
APOE
0.700 GeneticVariation UNIPROT APOE p.Leu167del mutation in familial hypercholesterolemia. 24267230

2013
dbSNP: rs769452
rs769452
APOE
0.700 GeneticVariation UNIPROT Description of a large family with autosomal dominant hypercholesterolemia associated with the APOE p.Leu167del mutation. 22949395

2013
dbSNP: rs769455
rs769455
APOE
0.700 GeneticVariation UNIPROT Description of a large family with autosomal dominant hypercholesterolemia associated with the APOE p.Leu167del mutation. 22949395

2013
dbSNP: rs769455
rs769455
APOE
0.700 GeneticVariation UNIPROT APOE p.Leu167del mutation in familial hypercholesterolemia. 24267230

2013
dbSNP: rs267606664
rs267606664
APOE
0.700 GeneticVariation UNIPROT

dbSNP: rs429358
rs429358
APOE
0.010 GeneticVariation BEFREE The current study aimed to investigate the genetic association between FH disease and ApoE gene polymorphisms (rs429358 and rs7412) in the Saudi population. 30235358

2018
dbSNP: rs7412
rs7412
APOE
0.010 GeneticVariation BEFREE The current study aimed to investigate the genetic association between FH disease and ApoE gene polymorphisms (rs429358 and rs7412) in the Saudi population. 30235358

2018
dbSNP: rs11542041
rs11542041
APOE
0.010 GeneticVariation BEFREE Compound heterozygotes for a novel mutation, apo E1 Nagoya (Arg142Ser) and Apo E2 (Arg158Cys), with severe type III hyperlipoproteinemia and familial hypercholesterolemia. 24953047

2014