rs5128
| Orientation | minus |
| Stabilized | minus |
| Make rs5128(C;C) |
| Make rs5128(C;G) |
| Make rs5128(G;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 11 |
| Position | 116832924 |
| Gene | APOC3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5128 |
| dbSNP (classic) | rs5128 |
| ClinGen | rs5128 |
| ebi | rs5128 |
| HLI | rs5128 |
| Exac | rs5128 |
| Gnomad | rs5128 |
| Varsome | rs5128 |
| LitVar | rs5128 |
| Map | rs5128 |
| PheGenI | rs5128 |
| Biobank | rs5128 |
| 1000 genomes | rs5128 |
| hgdp | rs5128 |
| ensembl | rs5128 |
| geneview | rs5128 |
| scholar | rs5128 |
| rs5128 | |
| pharmgkb | rs5128 |
| gwascentral | rs5128 |
| openSNP | rs5128 |
| 23andMe | rs5128 |
| SNPshot | rs5128 |
| SNPdbe | rs5128 |
| MSV3d | rs5128 |
| GWAS Ctlg | rs5128 |
| GMAF | 0.191 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
rs5128 (C3238G/3238C>G) is a SNP within the 3' UTR of APOC3 (Apolipoprotein C3).
[PMID 19424489
] subjects with GC/GG genotypes and diabetes exhibited sig. higher triglyceride (p=0.004), total cholesterol (p=0.003) and glucose (p=0.016) compared to CC subjects
[PMID 22848358] Hypercholesterolemia Is Associated with the Apolipoprotein C-III (APOC3) Genotype in Children Receiving HAART: An Eight-Year Retrospective Study
[PMID 17357073] Genetic analysis of 103 candidate genes for coronary artery disease and associated phenotypes in a founder population reveals a new association between endothelin-1 and high-density lipoprotein cholesterol.
[PMID 18513389] New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background.
[PMID 18789138] The APOA5 Trp19 allele is associated with metabolic syndrome via its association with plasma triglycerides.
[PMID 18801202] Genetic studies on the APOA1-C3-A5 gene cluster in Asian Indians with premature coronary artery disease.
[PMID 19014573] Application of two machine learning algorithms to genetic association studies in the presence of covariates.
[PMID 19041386] Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.
[PMID 19057464] Pharmacogenetic association of the APOA1/C3/A4/A5 gene cluster and lipid responses to fenofibrate: the genetics of lipid-lowering drugs and diet network study.
[PMID 19131662] A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.
[PMID 19263529] Genetic risk factors in recurrent venous thromboembolism: A multilocus, population-based, prospective approach.
[PMID 20406163] Fenofibrate and metabolic syndrome.
[PMID 22924697] Interactions between the apolipoprotein a1/c3/a5 haplotypes and alcohol consumption on serum lipid levels.
[PMID 23021345] Gene-diet interactions on plasma lipid levels in the Inuit population.
[PMID 25653052] Dietary patterns interact with APOA1/APOC3 polymorphisms to alter the risk of the metabolic syndrome: the Tehran Lipid and Glucose Study
[PMID 25928461] Associations of the APOC3 rs5128 polymorphism with plasma APOC3 and lipid levels: a meta-analysis
[PMID 26824674] Interactions of Environmental Factors and APOA1-APOC3-APOA4-APOA5 Gene Cluster Gene Polymorphisms with Metabolic Syndrome.
[PMID 27690381] Association of Apolipoprotein C3 Genetic Polymorphisms with the Risk of Ischemic Stroke in the Northern Chinese Han Population.
