rs2249891
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2249891(A;A) |
| Make rs2249891(A;G) |
| Make rs2249891(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 104861961 |
| Gene | ABCA1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2249891 |
| dbSNP (classic) | rs2249891 |
| ClinGen | rs2249891 |
| ebi | rs2249891 |
| HLI | rs2249891 |
| Exac | rs2249891 |
| Gnomad | rs2249891 |
| Varsome | rs2249891 |
| LitVar | rs2249891 |
| Map | rs2249891 |
| PheGenI | rs2249891 |
| Biobank | rs2249891 |
| 1000 genomes | rs2249891 |
| hgdp | rs2249891 |
| ensembl | rs2249891 |
| geneview | rs2249891 |
| scholar | rs2249891 |
| rs2249891 | |
| pharmgkb | rs2249891 |
| gwascentral | rs2249891 |
| openSNP | rs2249891 |
| 23andMe | rs2249891 |
| SNPshot | rs2249891 |
| SNPdbe | rs2249891 |
| MSV3d | rs2249891 |
| GWAS Ctlg | rs2249891 |
| GMAF | 0.331 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20855565
] Common genetic variation in multiple metabolic pathways influences susceptibility to low HDL-cholesterol and coronary heart disease
