rs1831281
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1831281(A;A) |
| Make rs1831281(A;G) |
| Make rs1831281(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 196711684 |
| Gene | CFH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1831281 |
| dbSNP (classic) | rs1831281 |
| ClinGen | rs1831281 |
| ebi | rs1831281 |
| HLI | rs1831281 |
| Exac | rs1831281 |
| Gnomad | rs1831281 |
| Varsome | rs1831281 |
| LitVar | rs1831281 |
| Map | rs1831281 |
| PheGenI | rs1831281 |
| Biobank | rs1831281 |
| 1000 genomes | rs1831281 |
| hgdp | rs1831281 |
| ensembl | rs1831281 |
| geneview | rs1831281 |
| scholar | rs1831281 |
| rs1831281 | |
| pharmgkb | rs1831281 |
| gwascentral | rs1831281 |
| openSNP | rs1831281 |
| 23andMe | rs1831281 |
| SNPshot | rs1831281 |
| SNPdbe | rs1831281 |
| MSV3d | rs1831281 |
| GWAS Ctlg | rs1831281 |
| GMAF | 0.247 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 19861685
] Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome.
