rs9868689
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9868689(C;C) |
| Make rs9868689(C;T) |
| Make rs9868689(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 39271450 |
| Gene | CX3CR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9868689 |
| dbSNP (classic) | rs9868689 |
| ClinGen | rs9868689 |
| ebi | rs9868689 |
| HLI | rs9868689 |
| Exac | rs9868689 |
| Gnomad | rs9868689 |
| Varsome | rs9868689 |
| LitVar | rs9868689 |
| Map | rs9868689 |
| PheGenI | rs9868689 |
| Biobank | rs9868689 |
| 1000 genomes | rs9868689 |
| hgdp | rs9868689 |
| ensembl | rs9868689 |
| geneview | rs9868689 |
| scholar | rs9868689 |
| rs9868689 | |
| pharmgkb | rs9868689 |
| gwascentral | rs9868689 |
| openSNP | rs9868689 |
| 23andMe | rs9868689 |
| SNPshot | rs9868689 |
| SNPdbe | rs9868689 |
| MSV3d | rs9868689 |
| GWAS Ctlg | rs9868689 |
| GMAF | 0.1263 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 24287500
] Prospective Study of Common Variants in CX3CR1 and Risk of Macular Degeneration: Pooled Analysis From 5 Long-term Studies
