rs1494961
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1494961(C;C) |
| Make rs1494961(C;T) |
| Make rs1494961(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 83453327 |
| Gene | HELQ |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1494961 |
| dbSNP (classic) | rs1494961 |
| ClinGen | rs1494961 |
| ebi | rs1494961 |
| HLI | rs1494961 |
| Exac | rs1494961 |
| Gnomad | rs1494961 |
| Varsome | rs1494961 |
| LitVar | rs1494961 |
| Map | rs1494961 |
| PheGenI | rs1494961 |
| Biobank | rs1494961 |
| 1000 genomes | rs1494961 |
| hgdp | rs1494961 |
| ensembl | rs1494961 |
| geneview | rs1494961 |
| scholar | rs1494961 |
| rs1494961 | |
| pharmgkb | rs1494961 |
| gwascentral | rs1494961 |
| openSNP | rs1494961 |
| 23andMe | rs1494961 |
| SNPshot | rs1494961 |
| SNPdbe | rs1494961 |
| MSV3d | rs1494961 |
| GWAS Ctlg | rs1494961 |
| GMAF | 0.3737 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21437268
] A Genome-Wide Association Study of Upper Aerodigestive Tract Cancers Conducted within the INHANCE Consortium
[PMID 23430454] Genetic variants at 4q21, 4q23 and 12q24 are associated with esophageal squamous cell carcinoma risk in a Chinese population
