rs6022786
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6022786(A;A) |
| Make rs6022786(A;G) |
| Make rs6022786(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 53830764 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6022786 |
| dbSNP (classic) | rs6022786 |
| ClinGen | rs6022786 |
| ebi | rs6022786 |
| HLI | rs6022786 |
| Exac | rs6022786 |
| Gnomad | rs6022786 |
| Varsome | rs6022786 |
| LitVar | rs6022786 |
| Map | rs6022786 |
| PheGenI | rs6022786 |
| Biobank | rs6022786 |
| 1000 genomes | rs6022786 |
| hgdp | rs6022786 |
| ensembl | rs6022786 |
| geneview | rs6022786 |
| scholar | rs6022786 |
| rs6022786 | |
| pharmgkb | rs6022786 |
| gwascentral | rs6022786 |
| openSNP | rs6022786 |
| 23andMe | rs6022786 |
| SNPshot | rs6022786 |
| SNPdbe | rs6022786 |
| MSV3d | rs6022786 |
| GWAS Ctlg | rs6022786 |
| GMAF | 0.4371 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22885925] |
| Trait | Polycystic ovary syndrome |
| Title | Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome. |
| Risk Allele | A |
| P-val | 2E-9 |
| Odds Ratio | 1.13 [NR] |
