rs1743966
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1743966(C;C) |
| Make rs1743966(C;T) |
| Make rs1743966(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 6 |
| Position | 134172809 |
| Gene | SGK1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1743966 |
| dbSNP (classic) | rs1743966 |
| ClinGen | rs1743966 |
| ebi | rs1743966 |
| HLI | rs1743966 |
| Exac | rs1743966 |
| Gnomad | rs1743966 |
| Varsome | rs1743966 |
| LitVar | rs1743966 |
| Map | rs1743966 |
| PheGenI | rs1743966 |
| Biobank | rs1743966 |
| 1000 genomes | rs1743966 |
| hgdp | rs1743966 |
| ensembl | rs1743966 |
| geneview | rs1743966 |
| scholar | rs1743966 |
| rs1743966 | |
| pharmgkb | rs1743966 |
| gwascentral | rs1743966 |
| openSNP | rs1743966 |
| 23andMe | rs1743966 |
| SNPshot | rs1743966 |
| SNPdbe | rs1743966 |
| MSV3d | rs1743966 |
| GWAS Ctlg | rs1743966 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 25709902
] A novel mutation of sgk-1 gene in central serous chorioretinopathy
