rs3769823
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs3769823(C;C) |
| Make rs3769823(C;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 2 |
| Position | 201258272 |
| Gene | CASP8 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3769823 |
| dbSNP (classic) | rs3769823 |
| ClinGen | rs3769823 |
| ebi | rs3769823 |
| HLI | rs3769823 |
| Exac | rs3769823 |
| Gnomad | rs3769823 |
| Varsome | rs3769823 |
| LitVar | rs3769823 |
| Map | rs3769823 |
| PheGenI | rs3769823 |
| Biobank | rs3769823 |
| 1000 genomes | rs3769823 |
| hgdp | rs3769823 |
| ensembl | rs3769823 |
| geneview | rs3769823 |
| scholar | rs3769823 |
| rs3769823 | |
| pharmgkb | rs3769823 |
| gwascentral | rs3769823 |
| openSNP | rs3769823 |
| 23andMe | rs3769823 |
| SNPshot | rs3769823 |
| SNPdbe | rs3769823 |
| MSV3d | rs3769823 |
| GWAS Ctlg | rs3769823 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 26635288
] Pathway, in silico and tissue-specific expression quantitative analyses of oesophageal squamous cell carcinoma genome-wide association studies data.
[PMID 28177523] Association between genetic variation within vitamin D receptor-DNA binding sites and risk of basal cell carcinoma.
[PMID 28542283] Shared susceptibility loci at 2q33 region for lung and esophageal cancers in high-incidence areas of esophageal cancer in northern China.
| ClinVar | |
|---|---|
| Risk | rs3769823(C;C) |
| Alt | rs3769823(C;C) |
| Reference | Rs3769823(T;T) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | CASP8 |
| CLNDBN | not specified |
| Reversed | 1 |
| HGVS | NC_000002.11:g.202122995A>G |
| CLNSRC | |
| CLNACC | RCV000455301.1, |
