rs284489
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs284489(A;A) |
| Make rs284489(A;G) |
| Make rs284489(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 104945792 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs284489 |
| dbSNP (classic) | rs284489 |
| ClinGen | rs284489 |
| ebi | rs284489 |
| HLI | rs284489 |
| Exac | rs284489 |
| Gnomad | rs284489 |
| Varsome | rs284489 |
| LitVar | rs284489 |
| Map | rs284489 |
| PheGenI | rs284489 |
| Biobank | rs284489 |
| 1000 genomes | rs284489 |
| hgdp | rs284489 |
| ensembl | rs284489 |
| geneview | rs284489 |
| scholar | rs284489 |
| rs284489 | |
| pharmgkb | rs284489 |
| gwascentral | rs284489 |
| openSNP | rs284489 |
| 23andMe | rs284489 |
| SNPshot | rs284489 |
| SNPdbe | rs284489 |
| MSV3d | rs284489 |
| GWAS Ctlg | rs284489 |
| GMAF | 0.4435 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22570617 ]
|
| Trait | |
| Title | Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. |
| Risk Allele | |
| P-val | 9E-10 |
| Odds Ratio | 1.6100 None |
