rs13016963
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs13016963(A;A) |
| Make rs13016963(A;G) |
| Make rs13016963(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 201298088 |
| Gene | ALS2CR12 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13016963 |
| dbSNP (classic) | rs13016963 |
| ClinGen | rs13016963 |
| ebi | rs13016963 |
| HLI | rs13016963 |
| Exac | rs13016963 |
| Gnomad | rs13016963 |
| Varsome | rs13016963 |
| LitVar | rs13016963 |
| Map | rs13016963 |
| PheGenI | rs13016963 |
| Biobank | rs13016963 |
| 1000 genomes | rs13016963 |
| hgdp | rs13016963 |
| ensembl | rs13016963 |
| geneview | rs13016963 |
| scholar | rs13016963 |
| rs13016963 | |
| pharmgkb | rs13016963 |
| gwascentral | rs13016963 |
| openSNP | rs13016963 |
| 23andMe | rs13016963 |
| SNPshot | rs13016963 |
| SNPdbe | rs13016963 |
| MSV3d | rs13016963 |
| GWAS Ctlg | rs13016963 |
| GMAF | 0.4027 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22323360
] Genotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: A meta-analysis of genome-wide association studies
| GWAS snp | |
|---|---|
| PMID | [PMID 21983787]
|
| Trait | |
| Title | Genome-wide association study identifies three new melanoma susceptibility loci. |
| Risk Allele | A |
| P-val | 9E-10 |
| Odds Ratio | 1.1400 None |
[PMID 26635288] Pathway, in silico and tissue-specific expression quantitative analyses of oesophageal squamous cell carcinoma genome-wide association studies data.
[PMID 28542283] Shared susceptibility loci at 2q33 region for lung and esophageal cancers in high-incidence areas of esophageal cancer in northern China.
