rs491567
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs491567(G;G) |
| Make rs491567(G;T) |
| Make rs491567(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 53654396 |
| Gene | WDR72 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs491567 |
| dbSNP (classic) | rs491567 |
| ClinGen | rs491567 |
| ebi | rs491567 |
| HLI | rs491567 |
| Exac | rs491567 |
| Gnomad | rs491567 |
| Varsome | rs491567 |
| LitVar | rs491567 |
| Map | rs491567 |
| PheGenI | rs491567 |
| Biobank | rs491567 |
| 1000 genomes | rs491567 |
| hgdp | rs491567 |
| ensembl | rs491567 |
| geneview | rs491567 |
| scholar | rs491567 |
| rs491567 | |
| pharmgkb | rs491567 |
| gwascentral | rs491567 |
| openSNP | rs491567 |
| 23andMe | rs491567 |
| SNPshot | rs491567 |
| SNPdbe | rs491567 |
| MSV3d | rs491567 |
| GWAS Ctlg | rs491567 |
| GMAF | 0.4036 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20383146 ]
|
| Trait | Chronic kidney disease |
| Title | New loci associated with kidney function and chronic kidney disease |
| Risk Allele | C |
| P-val | 3E-13 |
| Odds Ratio | 0.01 [0.005-0.013] ml/min/1.73 m2 increase |
