APOA1, apolipoprotein A1, 335

N. diseases: 416; N. variants: 32
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5072
rs5072
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0020557
Disease:
Hypertriglyceridemia
0.010 GeneticVariation BEFREE Logistic regression analysis revealed that rs5072, rs5128 and rs651821 were associated with hypertriglyceridemia, rs5104 and rs651821 were associated with low-HDL cholesterolemia in overall group. rs651821 was associated with hypertriglyceridemia and low-HDL cholesterolemia in both the male and female group. 30631647 2019
dbSNP: rs5072
rs5072
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0242339
Disease:
Dyslipidemias
0.010 GeneticVariation BEFREE Furthermore, the association of <i>APOA1</i> rs5072 in this gene cluster with dyslipidemia differed between genders; thus, additional studies are needed to confirm this conclusion, and the mechanisms underlying these results warrant further exploration. 30631647 2019
dbSNP: rs1217777010
rs1217777010
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0002726
Disease:
Amyloidosis
0.010 GeneticVariation BEFREE Glu34Lys is the only known charge inversion mutation in apoA-I that causes human amyloidosis. 30184436 2018
dbSNP: rs5070
rs5070
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0742343
Disease:
Acute Chest Syndrome
0.010 GeneticVariation BEFREE The rs670, rs5070 and rs693 polymorphisms are not genetic susceptibility factors for ACS in Mexican population and had no effect on their apolipoprotein concentrations. 28992985 2018
dbSNP: rs5070
rs5070
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0007222
Disease:
Cardiovascular Diseases
0.010 GeneticVariation BEFREE Lipid metabolism alterations contribute to acute coronary syndrome (ACS). rs670, rs5070 and rs693 polymorphisms have shown to modify the risk of cardiovascular disease. 28992985 2018
dbSNP: rs5070
rs5070
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0948089
Disease:
Acute Coronary Syndrome
0.010 GeneticVariation BEFREE Lipid metabolism alterations contribute to acute coronary syndrome (ACS). rs670, rs5070 and rs693 polymorphisms have shown to modify the risk of cardiovascular disease. 28992985 2018
dbSNP: rs670
rs670
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0007222
Disease:
Cardiovascular Diseases
0.010 GeneticVariation BEFREE Lipid metabolism alterations contribute to acute coronary syndrome (ACS). rs670, rs5070 and rs693 polymorphisms have shown to modify the risk of cardiovascular disease. 28992985 2018
dbSNP: rs670
rs670
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0948089
Disease:
Acute Coronary Syndrome
0.010 GeneticVariation BEFREE Lipid metabolism alterations contribute to acute coronary syndrome (ACS). rs670, rs5070 and rs693 polymorphisms have shown to modify the risk of cardiovascular disease. 28992985 2018
dbSNP: rs670
rs670
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0742343
Disease:
Acute Chest Syndrome
0.010 GeneticVariation BEFREE The rs670, rs5070 and rs693 polymorphisms are not genetic susceptibility factors for ACS in Mexican population and had no effect on their apolipoprotein concentrations. 28992985 2018
dbSNP: rs1799837
rs1799837
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE Carriers with rs670 G allele were more likely to get low HDL-C disease (OR = 1.46, OR95%CI: 1.118-1.915; P = 0.005); The genotypic and allelic frequencies of rs5069, rs5072, rs7116797, rs2070665, rs1799837 revealed no significant differences between cases and controls (P < 0.05); with reference to normal weight, Waist circumference (WC), Waist-to-hip ratio (WHR) individuals, respectively, general obesity measured by BMI had 2.686 times (OR95%CI: 1.695-4.256; P < 0.01), abdominal obesity measured by WC had 1.925 times (OR95%CI: 1.273-2.910; P = 0.002) and abdominal obesity measured by WHR had 1.640 times (OR95%CI: 1.114-2.416; P = 0.012) risk to get low HDL-C disease; APOA1 rs670 interacted with obesity (no matter general obesity or abdominal obesity) on low HDL-C disease. 28969676 2017
dbSNP: rs5069
rs5069
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE Carriers with rs670 G allele were more likely to get low HDL-C disease (OR = 1.46, OR95%CI: 1.118-1.915; P = 0.005); The genotypic and allelic frequencies of rs5069, rs5072, rs7116797, rs2070665, rs1799837 revealed no significant differences between cases and controls (P < 0.05); with reference to normal weight, Waist circumference (WC), Waist-to-hip ratio (WHR) individuals, respectively, general obesity measured by BMI had 2.686 times (OR95%CI: 1.695-4.256; P < 0.01), abdominal obesity measured by WC had 1.925 times (OR95%CI: 1.273-2.910; P = 0.002) and abdominal obesity measured by WHR had 1.640 times (OR95%CI: 1.114-2.416; P = 0.012) risk to get low HDL-C disease; APOA1 rs670 interacted with obesity (no matter general obesity or abdominal obesity) on low HDL-C disease. 28969676 2017
dbSNP: rs5070
rs5070
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C4699512
Disease:
Large-artery atherosclerosis (embolus/thrombosis)
0.010 GeneticVariation BEFREE Our findings suggested that genetic polymorphisms of ApoA1 rs5070 A/G may play a role in the susceptibility to LAA among male diabetic patients. 28238629 2017
dbSNP: rs5070
rs5070
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0038454
Disease:
Cerebrovascular accident
0.010 GeneticVariation BEFREE Apolipoprotein A1 rs5070 A/G polymorphism with stroke subtypes in Taiwan. 28238629 2017
dbSNP: rs632153
rs632153
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0242339
Disease:
Dyslipidemias
0.010 GeneticVariation BEFREE Most importantly, the variant rs632153 is involved in elevating TC, LDLC, TG and VLDLs and probably playing a crucial role in the manifestation of dyslipidemia. 28610615 2017
dbSNP: rs670
rs670
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0948008
Disease:
Ischemic stroke
0.010 GeneticVariation BEFREE A significantly increased risk for ischemic stroke was also identified among high-risk haplotypes (C-C-T-A and T-T-C-A) for rs670-rs2854116-rs2854117-rs662799. 28635360 2017
dbSNP: rs2070665
rs2070665
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0242339
Disease:
Dyslipidemias
0.010 GeneticVariation BEFREE These findings indicate that the polymorphisms in the APOA1 gene (rs670, rs5069, and rs2070665) are not associated with dyslipidemia in the Kazakh population assessed in this study. 27173266 2016
dbSNP: rs5069
rs5069
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0242339
Disease:
Dyslipidemias
0.010 GeneticVariation BEFREE These findings indicate that the polymorphisms in the APOA1 gene (rs670, rs5069, and rs2070665) are not associated with dyslipidemia in the Kazakh population assessed in this study. 27173266 2016
dbSNP: rs974389711
rs974389711
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0020473
Disease:
Hyperlipidemia
0.010 GeneticVariation BEFREE The various genotypes of the ApoA1 G75A SNP influence the efficacy of lipid regulation by pravastatin and policosanol in patients with hyperlipidemia. 27323196 2016
dbSNP: rs1384889210
rs1384889210
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0003850
Disease:
Arteriosclerosis
0.010 GeneticVariation BEFREE Expression of apoA-I(L141R)Pisa or apoA-I(L159R)FIN mutations in mice was associated with increased diet-induced atherosclerosis compared to either WT apoA-I transgenic or apoA-I(-/-) mice. 26363436 2015
dbSNP: rs1384889210
rs1384889210
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0004153
Disease:
Atherosclerosis
0.010 GeneticVariation BEFREE Expression of apoA-I(L141R)Pisa or apoA-I(L159R)FIN mutations in mice was associated with increased diet-induced atherosclerosis compared to either WT apoA-I transgenic or apoA-I(-/-) mice. 26363436 2015
dbSNP: rs632153
rs632153
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0410480
Disease:
Avascular Necrosis of Femur Head
0.010 GeneticVariation BEFREE We also identified rs632153 in ApoA1 gene was associated with increased risk of alcohol-induced ONFH using allele model (OR, 1.83; 95% CI, 1.16-2.88; P = 0.008) and log-additive model (adjusted OR, 1.77; 95% CI, 1.00-3.14; P = 0.046), analysis respectively. 26617857 2015
dbSNP: rs670
rs670
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0030567
Disease:
Parkinson Disease
0.010 GeneticVariation BEFREE Finally, evaluating rs670 genotype frequencies in 1,930 PD cases versus 997 NCs, the rs670 GG genotype shows a trend toward association (odds ratio: 1.1; P = 0.10) with PD. 25227208 2015
dbSNP: rs670
rs670
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE Our findings suggest that APOA1 rs670 indicate a post-surgery risk of breast cancer disease progression, and that carriers of this SNP may benefit from more advanced disease monitoring and therapy regimens than the current regular standards. 23829168 2013
dbSNP: rs670
rs670
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0521158
Disease:
Recurrent tumor
0.010 GeneticVariation BEFREE Moreover, rs670 A/A carrying patients had higher risks in both tumor recurrence (HR=3.12, 95% CI=1.29-7.56, p=0.012) and mortality (HR=4.36, 95% CI=1.52-12.47, p=0.006) than patients with no A alleles after adjustments for associated baseline parameters. 23829168 2013
dbSNP: rs670
rs670
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE Our findings suggest that APOA1 rs670 indicate a post-surgery risk of breast cancer disease progression, and that carriers of this SNP may benefit from more advanced disease monitoring and therapy regimens than the current regular standards. 23829168 2013