rs12144939
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12144939(G;G) |
| Make rs12144939(G;T) |
| Make rs12144939(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 196729815 |
| Gene | CFH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12144939 |
| dbSNP (classic) | rs12144939 |
| ClinGen | rs12144939 |
| ebi | rs12144939 |
| HLI | rs12144939 |
| Exac | rs12144939 |
| Gnomad | rs12144939 |
| Varsome | rs12144939 |
| LitVar | rs12144939 |
| Map | rs12144939 |
| PheGenI | rs12144939 |
| Biobank | rs12144939 |
| 1000 genomes | rs12144939 |
| hgdp | rs12144939 |
| ensembl | rs12144939 |
| geneview | rs12144939 |
| scholar | rs12144939 |
| rs12144939 | |
| pharmgkb | rs12144939 |
| gwascentral | rs12144939 |
| openSNP | rs12144939 |
| 23andMe | rs12144939 |
| SNPshot | rs12144939 |
| SNPdbe | rs12144939 |
| MSV3d | rs12144939 |
| GWAS Ctlg | rs12144939 |
| GMAF | 0.1905 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21882633] [Influence of genetic mutations on clinical presentation of subretinal neovascularization. Report 1: The impact of CFH and IL-8 genes polymorphism]
[PMID 24675670
] Impact of the common genetic associations of age-related macular degeneration upon systemic complement component C3d levels
