rs611917
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs611917(C;C) |
| Make rs611917(C;T) |
| Make rs611917(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 109272630 |
| Gene | CELSR2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs611917 |
| dbSNP (classic) | rs611917 |
| ClinGen | rs611917 |
| ebi | rs611917 |
| HLI | rs611917 |
| Exac | rs611917 |
| Gnomad | rs611917 |
| Varsome | rs611917 |
| LitVar | rs611917 |
| Map | rs611917 |
| PheGenI | rs611917 |
| Biobank | rs611917 |
| 1000 genomes | rs611917 |
| hgdp | rs611917 |
| ensembl | rs611917 |
| geneview | rs611917 |
| scholar | rs611917 |
| rs611917 | |
| pharmgkb | rs611917 |
| gwascentral | rs611917 |
| openSNP | rs611917 |
| 23andMe | rs611917 |
| SNPshot | rs611917 |
| SNPdbe | rs611917 |
| MSV3d | rs611917 |
| GWAS Ctlg | rs611917 |
| GMAF | 0.2498 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23050023
] Association of genetic variants influencing lipid levels with coronary artery disease in Japanese individuals
[PMID 18262040] LDL-cholesterol concentrations: a genome-wide association study.
