rs112000638
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs112000638(C;C) |
| Make rs112000638(C;T) |
| Make rs112000638(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 131359434 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs112000638 |
| dbSNP (classic) | rs112000638 |
| ClinGen | rs112000638 |
| ebi | rs112000638 |
| HLI | rs112000638 |
| Exac | rs112000638 |
| Gnomad | rs112000638 |
| Varsome | rs112000638 |
| LitVar | rs112000638 |
| Map | rs112000638 |
| PheGenI | rs112000638 |
| Biobank | rs112000638 |
| 1000 genomes | rs112000638 |
| hgdp | rs112000638 |
| ensembl | rs112000638 |
| geneview | rs112000638 |
| scholar | rs112000638 |
| rs112000638 | |
| pharmgkb | rs112000638 |
| gwascentral | rs112000638 |
| openSNP | rs112000638 |
| 23andMe | rs112000638 |
| SNPshot | rs112000638 |
| SNPdbe | rs112000638 |
| MSV3d | rs112000638 |
| GWAS Ctlg | rs112000638 |
| GMAF | 0.005969 |
| Max Magnitude | 0 |
[PMID 23534868] CFH (rs1410996), HTRA1 (rs112000638) and ARMS2 (rs10490923) Gene Polymorphisms are Associated with AMD Risk in Spanish Patients
