rs267738
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs267738(A;A) |
| Make rs267738(A;C) |
| Make rs267738(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 150968149 |
| Gene | CERS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs267738 |
| dbSNP (classic) | rs267738 |
| ClinGen | rs267738 |
| ebi | rs267738 |
| HLI | rs267738 |
| Exac | rs267738 |
| Gnomad | rs267738 |
| Varsome | rs267738 |
| LitVar | rs267738 |
| Map | rs267738 |
| PheGenI | rs267738 |
| Biobank | rs267738 |
| 1000 genomes | rs267738 |
| hgdp | rs267738 |
| ensembl | rs267738 |
| geneview | rs267738 |
| scholar | rs267738 |
| rs267738 | |
| pharmgkb | rs267738 |
| gwascentral | rs267738 |
| openSNP | rs267738 |
| 23andMe | rs267738 |
| SNPshot | rs267738 |
| SNPdbe | rs267738 |
| MSV3d | rs267738 |
| GWAS Ctlg | rs267738 |
| GMAF | 0.09917 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 23585552] Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment
