rs4520
Orientation | plus |
Stabilized | plus |
Make rs4520(C;C) |
Make rs4520(C;T) |
Make rs4520(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 116830819 |
Gene | APOC3 |
is a | snp |
is | mentioned by |
dbSNP | rs4520 |
dbSNP (classic) | rs4520 |
ClinGen | rs4520 |
ebi | rs4520 |
HLI | rs4520 |
Exac | rs4520 |
Gnomad | rs4520 |
Varsome | rs4520 |
LitVar | rs4520 |
Map | rs4520 |
PheGenI | rs4520 |
Biobank | rs4520 |
1000 genomes | rs4520 |
hgdp | rs4520 |
ensembl | rs4520 |
geneview | rs4520 |
scholar | rs4520 |
rs4520 | |
pharmgkb | rs4520 |
gwascentral | rs4520 |
openSNP | rs4520 |
23andMe | rs4520 |
SNPshot | rs4520 |
SNPdbe | rs4520 |
MSV3d | rs4520 |
GWAS Ctlg | rs4520 |
GMAF | 0.3779 |
Max Magnitude | 0 |
[PMID 19592705] Effects of variations in the APOA1/C3/A4/A5 gene cluster on different parameters of postprandial lipid metabolism in healthy young men
[PMID 16417409] Associations among race/ethnicity, ApoC-III genotypes, and lipids in HIV-1-infected individuals on antiretroviral therapy.
[PMID 16700901] Physiogenomic analysis of weight loss induced by dietary carbohydrate restriction.
[PMID 18513389] New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background.
[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 27690381] Association of Apolipoprotein C3 Genetic Polymorphisms with the Risk of Ischemic Stroke in the Northern Chinese Han Population.