rs17194885
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17194885(A;A) |
| Make rs17194885(A;C) |
| Make rs17194885(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 37439987 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17194885 |
| dbSNP (classic) | rs17194885 |
| ClinGen | rs17194885 |
| ebi | rs17194885 |
| HLI | rs17194885 |
| Exac | rs17194885 |
| Gnomad | rs17194885 |
| Varsome | rs17194885 |
| LitVar | rs17194885 |
| Map | rs17194885 |
| PheGenI | rs17194885 |
| Biobank | rs17194885 |
| 1000 genomes | rs17194885 |
| hgdp | rs17194885 |
| ensembl | rs17194885 |
| geneview | rs17194885 |
| scholar | rs17194885 |
| rs17194885 | |
| pharmgkb | rs17194885 |
| gwascentral | rs17194885 |
| openSNP | rs17194885 |
| 23andMe | rs17194885 |
| SNPshot | rs17194885 |
| SNPdbe | rs17194885 |
| MSV3d | rs17194885 |
| GWAS Ctlg | rs17194885 |
| GMAF | 0.1198 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23393555 ]
|
| Trait | Retinopathy in non-diabetics |
| Title | Genome-wide association study of retinopathy in individuals without diabetes. |
| Risk Allele | A |
| P-val | 4E-6 |
| Odds Ratio | .61 [0.36-0.86] unit decrease |
