rs7893395
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs7893395(C;T) |
| Make rs7893395(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 16863501 |
| Gene | CUBN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7893395 |
| dbSNP (classic) | rs7893395 |
| ClinGen | rs7893395 |
| ebi | rs7893395 |
| HLI | rs7893395 |
| Exac | rs7893395 |
| Gnomad | rs7893395 |
| Varsome | rs7893395 |
| LitVar | rs7893395 |
| Map | rs7893395 |
| PheGenI | rs7893395 |
| Biobank | rs7893395 |
| 1000 genomes | rs7893395 |
| hgdp | rs7893395 |
| ensembl | rs7893395 |
| geneview | rs7893395 |
| scholar | rs7893395 |
| rs7893395 | |
| pharmgkb | rs7893395 |
| gwascentral | rs7893395 |
| openSNP | rs7893395 |
| 23andMe | rs7893395 |
| SNPshot | rs7893395 |
| SNPdbe | rs7893395 |
| MSV3d | rs7893395 |
| GWAS Ctlg | rs7893395 |
| GMAF | 0.3242 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20855565
] Common genetic variation in multiple metabolic pathways influences susceptibility to low HDL-cholesterol and coronary heart disease
