rs2284664
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2284664(A;A) |
| Make rs2284664(A;G) |
| Make rs2284664(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 196733395 |
| Gene | CFH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2284664 |
| dbSNP (classic) | rs2284664 |
| ClinGen | rs2284664 |
| ebi | rs2284664 |
| HLI | rs2284664 |
| Exac | rs2284664 |
| Gnomad | rs2284664 |
| Varsome | rs2284664 |
| LitVar | rs2284664 |
| Map | rs2284664 |
| PheGenI | rs2284664 |
| Biobank | rs2284664 |
| 1000 genomes | rs2284664 |
| hgdp | rs2284664 |
| ensembl | rs2284664 |
| geneview | rs2284664 |
| scholar | rs2284664 |
| rs2284664 | |
| pharmgkb | rs2284664 |
| gwascentral | rs2284664 |
| openSNP | rs2284664 |
| 23andMe | rs2284664 |
| SNPshot | rs2284664 |
| SNPdbe | rs2284664 |
| MSV3d | rs2284664 |
| GWAS Ctlg | rs2284664 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
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[PMID 26217379
] Ancestry of the Timorese: age-related macular degeneration associated genotype and allele sharing among human populations from throughout the world
[PMID 26296146] PREVALENCE OF THE COMPLEMENT FACTOR H AND GSTM1 GENES POLYMORPHISMS IN PATIENTS WITH CENTRAL SEROUS CHORIORETINOPATHY
