rs7524776
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7524776(C;C) |
| Make rs7524776(C;T) |
| Make rs7524776(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 196654207 |
| Gene | CFH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7524776 |
| dbSNP (classic) | rs7524776 |
| ClinGen | rs7524776 |
| ebi | rs7524776 |
| HLI | rs7524776 |
| Exac | rs7524776 |
| Gnomad | rs7524776 |
| Varsome | rs7524776 |
| LitVar | rs7524776 |
| Map | rs7524776 |
| PheGenI | rs7524776 |
| Biobank | rs7524776 |
| 1000 genomes | rs7524776 |
| hgdp | rs7524776 |
| ensembl | rs7524776 |
| geneview | rs7524776 |
| scholar | rs7524776 |
| rs7524776 | |
| pharmgkb | rs7524776 |
| gwascentral | rs7524776 |
| openSNP | rs7524776 |
| 23andMe | rs7524776 |
| SNPshot | rs7524776 |
| SNPdbe | rs7524776 |
| MSV3d | rs7524776 |
| GWAS Ctlg | rs7524776 |
| GMAF | 0.118 |
| Max Magnitude | 0 |
| ? | (C;C) (C;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]
