Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11542041
rs11542041
0.010 GeneticVariation BEFREE This explains the significant effect of the apoE gene locus on the variability of plasma lipoprotein concentrations and moreover the implication of apoE alleles in the aetiology of multifactorial forms of hyperlipidaemia e.g. familial type III hyperlipidaemia (apoE2; arg158----cys) and polygenic hypercholesterolaemia (apoE4; cys112----arg). 3141688

1988

dbSNP: rs429358
rs429358
0.010 GeneticVariation BEFREE This explains the significant effect of the apoE gene locus on the variability of plasma lipoprotein concentrations and moreover the implication of apoE alleles in the aetiology of multifactorial forms of hyperlipidaemia e.g. familial type III hyperlipidaemia (apoE2; arg158----cys) and polygenic hypercholesterolaemia (apoE4; cys112----arg). 3141688

1988

dbSNP: rs268
rs268
LPL
0.010 GeneticVariation BEFREE Our data suggest that the Asn 291-->Ser substitution is likely to be a significant predisposing factor contributing to the expression of different forms of hyperlipidemia when associated with other genetic factors such as the presence of apoE2. 7583546

1995

dbSNP: rs573658040
rs573658040
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

dbSNP: rs769455
rs769455
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

dbSNP: rs267606661
rs267606661
0.010 GeneticVariation BEFREE In relatives of the proband, APOE R112; R251G was consistently found in subjects with both hyperlipidemia and atherosclerosis. 9360638

1997

dbSNP: rs140808909
rs140808909
0.010 GeneticVariation BEFREE Characterization of apolipoprotein E7 (Glu(244)-->Lys, Glu(245)--->Lys), a mutant apolipoprotein E associated with hyperlipidemia and atherosclerosis. 9925654

1999

dbSNP: rs879254840
rs879254840
0.010 GeneticVariation BEFREE Characterization of apolipoprotein E7 (Glu(244)-->Lys, Glu(245)--->Lys), a mutant apolipoprotein E associated with hyperlipidemia and atherosclerosis. 9925654

1999

dbSNP: rs1799945
rs1799945
0.010 GeneticVariation BEFREE We determined the age; sex; presence of IRS (1 or more of the following: body mass index of >25, diabetes, or hyperlipidemia); serum iron tests and liver iron concentration (LIC; reference value, <36 micromol/g); liver function test results; C282Y and H63D HFE mutations; and liver histological status. 10535879

1999

dbSNP: rs1800562
rs1800562
0.010 GeneticVariation BEFREE We determined the age; sex; presence of IRS (1 or more of the following: body mass index of >25, diabetes, or hyperlipidemia); serum iron tests and liver iron concentration (LIC; reference value, <36 micromol/g); liver function test results; C282Y and H63D HFE mutations; and liver histological status. 10535879

1999

dbSNP: rs3829462
rs3829462
0.010 GeneticVariation BEFREE These results show an association of the missense mutations Val-73-Met and Leu-334-Phe as susceptibility alleles for combined forms of hyperlipidemia. 10606208

1999

dbSNP: rs6078
rs6078
0.010 GeneticVariation BEFREE These results show an association of the missense mutations Val-73-Met and Leu-334-Phe as susceptibility alleles for combined forms of hyperlipidemia. 10606208

1999

dbSNP: rs1800206
rs1800206
0.020 GeneticVariation BEFREE This study examined the effect a polymorphism (L162V) in the gene for peroxisome proliferator activated receptor (PPAR) alpha in the development of non-insulin-dependent diabetes mellitus (type 2 DM), obesity and hyperlipidaemia. 11409711

2001

dbSNP: rs4994
rs4994
0.020 GeneticVariation BEFREE In conclusion, no major difference was associated with the beta3AR Trp64Arg or FABP2 Ala54Thr polymorphism in terms of type 2 diabetes or hyperlipidemia in young to older Japanese men. 11699048

2001

dbSNP: rs1799883
rs1799883
0.010 GeneticVariation BEFREE In conclusion, no major difference was associated with the beta3AR Trp64Arg or FABP2 Ala54Thr polymorphism in terms of type 2 diabetes or hyperlipidemia in young to older Japanese men. 11699048

2001

dbSNP: rs773641005
rs773641005
0.010 GeneticVariation BEFREE In conclusion, no major difference was associated with the beta3AR Trp64Arg or FABP2 Ala54Thr polymorphism in terms of type 2 diabetes or hyperlipidemia in young to older Japanese men. 11699048

2001

dbSNP: rs121918392
rs121918392
0.010 GeneticVariation BEFREE A case of hyperlipidemia with homozygous apolipoprotein E5 (Glu3-->Lys). 12069856

2002

dbSNP: rs1341991169
rs1341991169
LPL
0.010 GeneticVariation BEFREE A case of hyperlipidemia with homozygous apolipoprotein E5 (Glu3-->Lys). 12069856

2002

dbSNP: rs2230806
rs2230806
0.010 GeneticVariation BEFREE In conclusion, we provide additional evidence that the R219K polymorphism in the ABCA1 gene either directly or as a result of linkage disequilibrium with additional functional variant(s), has a protective effect against CHD and is associated with lower plasma triglycerides in sub-groups of patients with hyperlipidaemia. 12700893

2003

dbSNP: rs4994
rs4994
0.020 GeneticVariation BEFREE To determine whether this SNP affects insulin resistance syndrome associated with type 2 diabetes, we examined its effects on susceptibility to obesity, hyperlipidemia and hypertension in type 2 diabetic subjects and on susceptibility to type 2 diabetes by interaction with other frequent genes involved in lipid metabolism, namely, beta3-adrenergic receptor (b3AR) Trp64Arg, phosphodiesterase 3B (PDE3B) c.1389G>A or lysosomal acid lipase (LAL) Thr-6Pro. 12965109

2003

dbSNP: rs4757268
rs4757268
0.010 GeneticVariation BEFREE To determine whether this SNP affects insulin resistance syndrome associated with type 2 diabetes, we examined its effects on susceptibility to obesity, hyperlipidemia and hypertension in type 2 diabetic subjects and on susceptibility to type 2 diabetes by interaction with other frequent genes involved in lipid metabolism, namely, beta3-adrenergic receptor (b3AR) Trp64Arg, phosphodiesterase 3B (PDE3B) c.1389G>A or lysosomal acid lipase (LAL) Thr-6Pro. 12965109

2003

dbSNP: rs2228314
rs2228314
0.010 GeneticVariation BEFREE Further work is necessary to confirm the role of 1784G>C in the development of hyperlipidemia. 15547298

2005

dbSNP: rs150599989
rs150599989
0.010 GeneticVariation BEFREE Identification of a novel C5L2 variant (S323I) in a French Canadian family with familial combined hyperlipemia. 16627811

2006

dbSNP: rs920435389
rs920435389
0.010 GeneticVariation BEFREE Multivariate logistic regression analysis after adjustments for age, body mass index, present illness (hyperlipidemia and diabetes mellitus), and lifestyle (smoking and drinking) showed -22A>G to have an association with hypertension in men (AA vs. AG+GG: odds ratio=1.27; 95% confidence interval: 1.02-1.57; P=0.030). 18075463

2007

dbSNP: rs1805087
rs1805087
MTR
0.010 GeneticVariation BEFREE Further study is needed to confirm the role of HHcy and MS A2756G mutation in the development of hyperlipidemia. 19263808

2008