rs9615362
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs9615362(A;A) |
| Make rs9615362(A;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 46399244 |
| Gene | CELSR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9615362 |
| dbSNP (classic) | rs9615362 |
| ClinGen | rs9615362 |
| ebi | rs9615362 |
| HLI | rs9615362 |
| Exac | rs9615362 |
| Gnomad | rs9615362 |
| Varsome | rs9615362 |
| LitVar | rs9615362 |
| Map | rs9615362 |
| PheGenI | rs9615362 |
| Biobank | rs9615362 |
| 1000 genomes | rs9615362 |
| hgdp | rs9615362 |
| ensembl | rs9615362 |
| geneview | rs9615362 |
| scholar | rs9615362 |
| rs9615362 | |
| pharmgkb | rs9615362 |
| gwascentral | rs9615362 |
| openSNP | rs9615362 |
| 23andMe | rs9615362 |
| SNPshot | rs9615362 |
| SNPdbe | rs9615362 |
| MSV3d | rs9615362 |
| GWAS Ctlg | rs9615362 |
| GMAF | 0.2098 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 19403135] Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study
Mentioned in retracted [PMID 20595579]
