rs3813627
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3813627(G;G) |
| Make rs3813627(G;T) |
| Make rs3813627(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 161225358 |
| Gene | APOA2, MIR5187, TOMM40L |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3813627 |
| dbSNP (classic) | rs3813627 |
| ClinGen | rs3813627 |
| ebi | rs3813627 |
| HLI | rs3813627 |
| Exac | rs3813627 |
| Gnomad | rs3813627 |
| Varsome | rs3813627 |
| LitVar | rs3813627 |
| Map | rs3813627 |
| PheGenI | rs3813627 |
| Biobank | rs3813627 |
| 1000 genomes | rs3813627 |
| hgdp | rs3813627 |
| ensembl | rs3813627 |
| geneview | rs3813627 |
| scholar | rs3813627 |
| rs3813627 | |
| pharmgkb | rs3813627 |
| gwascentral | rs3813627 |
| openSNP | rs3813627 |
| 23andMe | rs3813627 |
| SNPshot | rs3813627 |
| SNPdbe | rs3813627 |
| MSV3d | rs3813627 |
| GWAS Ctlg | rs3813627 |
| GMAF | 0.3375 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20855565
] Common genetic variation in multiple metabolic pathways influences susceptibility to low HDL-cholesterol and coronary heart disease
[PMID 19878569] Candidate genetic analysis of plasma high-density lipoprotein-cholesterol and severity of coronary atherosclerosis.
