rs960531
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs960531(C;C) |
| Make rs960531(C;G) |
| Make rs960531(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 83965543 |
| Gene | DLG2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs960531 |
| dbSNP (classic) | rs960531 |
| ClinGen | rs960531 |
| ebi | rs960531 |
| HLI | rs960531 |
| Exac | rs960531 |
| Gnomad | rs960531 |
| Varsome | rs960531 |
| LitVar | rs960531 |
| Map | rs960531 |
| PheGenI | rs960531 |
| Biobank | rs960531 |
| 1000 genomes | rs960531 |
| hgdp | rs960531 |
| ensembl | rs960531 |
| geneview | rs960531 |
| scholar | rs960531 |
| rs960531 | |
| pharmgkb | rs960531 |
| gwascentral | rs960531 |
| openSNP | rs960531 |
| 23andMe | rs960531 |
| SNPshot | rs960531 |
| SNPdbe | rs960531 |
| MSV3d | rs960531 |
| GWAS Ctlg | rs960531 |
| GMAF | 0.06979 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20378690] Genetic variants in selenoprotein genes increase risk of colorectal cancer
