rs876660771
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 6.7 | CDH1-based gastric cancer risk |
| Make rs876660771(A;A) |
| Chromosome | 16 |
| Position | 68812264 |
| Gene | CDH1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs876660771 |
| dbSNP (classic) | rs876660771 |
| ClinGen | rs876660771 |
| ebi | rs876660771 |
| HLI | rs876660771 |
| Exac | rs876660771 |
| Gnomad | rs876660771 |
| Varsome | rs876660771 |
| LitVar | rs876660771 |
| Map | rs876660771 |
| PheGenI | rs876660771 |
| Biobank | rs876660771 |
| 1000 genomes | rs876660771 |
| hgdp | rs876660771 |
| ensembl | rs876660771 |
| geneview | rs876660771 |
| scholar | rs876660771 |
| rs876660771 | |
| pharmgkb | rs876660771 |
| gwascentral | rs876660771 |
| openSNP | rs876660771 |
| 23andMe | rs876660771 |
| SNPshot | rs876660771 |
| SNPdbe | rs876660771 |
| MSV3d | rs876660771 |
| GWAS Ctlg | rs876660771 |
| Max Magnitude | 6.7 |
Also known as c.1137+1G>A, the minor allele is considered a pathogenic rare mutation for hereditary diffuse gastric cancer in ClinVar.
| ClinVar | |
|---|---|
| Risk | rs876660771(A;A) |
| Alt | rs876660771(A;A) |
| Reference | Rs876660771(G;G) |
| Significance | Pathogenic |
| Disease | Hereditary cancer-predisposing syndrome Hereditary diffuse gastric cancer not provided |
| Variation | info |
| Gene | CDH1 |
| CLNDBN | Hereditary cancer-predisposing syndrome Hereditary diffuse gastric cancer not provided |
| Reversed | 0 |
| HGVS | NC_000016.9:g.68846167G>A |
| CLNSRC | |
| CLNACC | RCV000219632.1, RCV000230827.2, RCV000483444.1, |
