rs10750097
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10750097(A;A) |
| Make rs10750097(A;G) |
| Make rs10750097(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 116793324 |
| Gene | APOA5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10750097 |
| dbSNP (classic) | rs10750097 |
| ClinGen | rs10750097 |
| ebi | rs10750097 |
| HLI | rs10750097 |
| Exac | rs10750097 |
| Gnomad | rs10750097 |
| Varsome | rs10750097 |
| LitVar | rs10750097 |
| Map | rs10750097 |
| PheGenI | rs10750097 |
| Biobank | rs10750097 |
| 1000 genomes | rs10750097 |
| hgdp | rs10750097 |
| ensembl | rs10750097 |
| geneview | rs10750097 |
| scholar | rs10750097 |
| rs10750097 | |
| pharmgkb | rs10750097 |
| gwascentral | rs10750097 |
| openSNP | rs10750097 |
| 23andMe | rs10750097 |
| SNPshot | rs10750097 |
| SNPdbe | rs10750097 |
| MSV3d | rs10750097 |
| GWAS Ctlg | rs10750097 |
| GMAF | 0.3416 |
| Max Magnitude | 0 |
[PMID 21889769
] Variants in the APOA5 gene region and the response to combination therapy with statins and fenofibric acid in a randomized clinical trial of individuals with mixed dyslipidemia
[PMID 16670016] Allelic drop-out may occur with a primer binding site polymorphism for the commonly used RFLP assay for the -1131T>C polymorphism of the Apolipoprotein AV gene.
[PMID 19041386] Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.
[PMID 22425169] Vitamin D dependent effects of APOA5 polymorphisms on HDL cholesterol.
[PMID 24402875] Genetic association of lipid metabolism related SNPs with myocardial infarction in the Pakistani population
