rs6007897
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs6007897(C;C) |
| Make rs6007897(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 46384624 |
| Gene | CELSR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6007897 |
| dbSNP (classic) | rs6007897 |
| ClinGen | rs6007897 |
| ebi | rs6007897 |
| HLI | rs6007897 |
| Exac | rs6007897 |
| Gnomad | rs6007897 |
| Varsome | rs6007897 |
| LitVar | rs6007897 |
| Map | rs6007897 |
| PheGenI | rs6007897 |
| Biobank | rs6007897 |
| 1000 genomes | rs6007897 |
| hgdp | rs6007897 |
| ensembl | rs6007897 |
| geneview | rs6007897 |
| scholar | rs6007897 |
| rs6007897 | |
| pharmgkb | rs6007897 |
| gwascentral | rs6007897 |
| openSNP | rs6007897 |
| 23andMe | rs6007897 |
| SNPshot | rs6007897 |
| SNPdbe | rs6007897 |
| MSV3d | rs6007897 |
| GWAS Ctlg | rs6007897 |
| GMAF | 0.2227 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19403135] Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study
[PMID 18454203
] Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression.
[PMID 26480662] [Association Between SNP rs6007897 of CELSR1 and Acute Ischemic Stroke in Western China Han Population: a Case-control Study]
