rs7018475
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7018475(G;G) |
| Make rs7018475(G;T) |
| Make rs7018475(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 22137686 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7018475 |
| dbSNP (classic) | rs7018475 |
| ClinGen | rs7018475 |
| ebi | rs7018475 |
| HLI | rs7018475 |
| Exac | rs7018475 |
| Gnomad | rs7018475 |
| Varsome | rs7018475 |
| LitVar | rs7018475 |
| Map | rs7018475 |
| PheGenI | rs7018475 |
| Biobank | rs7018475 |
| 1000 genomes | rs7018475 |
| hgdp | rs7018475 |
| ensembl | rs7018475 |
| geneview | rs7018475 |
| scholar | rs7018475 |
| rs7018475 | |
| pharmgkb | rs7018475 |
| gwascentral | rs7018475 |
| openSNP | rs7018475 |
| 23andMe | rs7018475 |
| SNPshot | rs7018475 |
| SNPdbe | rs7018475 |
| MSV3d | rs7018475 |
| GWAS Ctlg | rs7018475 |
| GMAF | 0.2984 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22293688 ]
|
| Trait | |
| Title | 1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data. |
| Risk Allele | |
| P-val | 3E-8 |
| Odds Ratio | 1.3500 None |
