rs202115589
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs202115589(C;C) |
| Make rs202115589(C;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 16 |
| Position | 68819424 |
| Gene | CDH1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs202115589 |
| dbSNP (classic) | rs202115589 |
| ClinGen | rs202115589 |
| ebi | rs202115589 |
| HLI | rs202115589 |
| Exac | rs202115589 |
| Gnomad | rs202115589 |
| Varsome | rs202115589 |
| LitVar | rs202115589 |
| Map | rs202115589 |
| PheGenI | rs202115589 |
| Biobank | rs202115589 |
| 1000 genomes | rs202115589 |
| hgdp | rs202115589 |
| ensembl | rs202115589 |
| geneview | rs202115589 |
| scholar | rs202115589 |
| rs202115589 | |
| pharmgkb | rs202115589 |
| gwascentral | rs202115589 |
| openSNP | rs202115589 |
| 23andMe | rs202115589 |
| SNPshot | rs202115589 |
| SNPdbe | rs202115589 |
| MSV3d | rs202115589 |
| GWAS Ctlg | rs202115589 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs202115589(C;C) |
| Alt | rs202115589(C;C) |
| Reference | Rs202115589(T;T) |
| Significance | Probable-non-pathogenic |
| Disease | not specified Hereditary diffuse gastric cancer |
| Variation | info |
| Gene | CDH1 |
| CLNDBN | not specified Hereditary diffuse gastric cancer |
| Reversed | 0 |
| HGVS | NC_000016.9:g.68853327T>C |
| CLNSRC | |
| CLNACC | RCV000442492.1, RCV000467987.1, |
