rs6698843
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6698843(C;C) |
| Make rs6698843(C;T) |
| Make rs6698843(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 1 |
| Position | 109264212 |
| Gene | CELSR2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6698843 |
| dbSNP (classic) | rs6698843 |
| ClinGen | rs6698843 |
| ebi | rs6698843 |
| HLI | rs6698843 |
| Exac | rs6698843 |
| Gnomad | rs6698843 |
| Varsome | rs6698843 |
| LitVar | rs6698843 |
| Map | rs6698843 |
| PheGenI | rs6698843 |
| Biobank | rs6698843 |
| 1000 genomes | rs6698843 |
| hgdp | rs6698843 |
| ensembl | rs6698843 |
| geneview | rs6698843 |
| scholar | rs6698843 |
| rs6698843 | |
| pharmgkb | rs6698843 |
| gwascentral | rs6698843 |
| openSNP | rs6698843 |
| 23andMe | rs6698843 |
| SNPshot | rs6698843 |
| SNPdbe | rs6698843 |
| MSV3d | rs6698843 |
| GWAS Ctlg | rs6698843 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 26464717
] Association of variants in CELSR2-PSRC1-SORT1 with risk of serum lipid traits, coronary artery disease and ischemic stroke
