rs876658865
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Geno | Mag | Summary | 
|---|---|---|
| (CCC;CCC) | 0 | common in clinvar | 
| Chromosome | 16 | 
| Position | 68738372 | 
| Gene | CDH1 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs876658865 | 
| dbSNP (classic) | rs876658865 | 
| ClinGen | rs876658865 | 
| ebi | rs876658865 | 
| HLI | rs876658865 | 
| Exac | rs876658865 | 
| Gnomad | rs876658865 | 
| Varsome | rs876658865 | 
| LitVar | rs876658865 | 
| Map | rs876658865 | 
| PheGenI | rs876658865 | 
| Biobank | rs876658865 | 
| 1000 genomes | rs876658865 | 
| hgdp | rs876658865 | 
| ensembl | rs876658865 | 
| geneview | rs876658865 | 
| scholar | rs876658865 | 
| rs876658865 | |
| pharmgkb | rs876658865 | 
| gwascentral | rs876658865 | 
| openSNP | rs876658865 | 
| 23andMe | rs876658865 | 
| SNPshot | rs876658865 | 
| SNPdbe | rs876658865 | 
| MSV3d | rs876658865 | 
| GWAS Ctlg | rs876658865 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs876658865(T;T) | 
| Alt | rs876658865(T;T) | 
| Reference | Rs876658865(CCC;CCC) | 
| Significance | Pathogenic | 
| Disease | Hereditary cancer-predisposing syndrome | 
| Variation | info | 
| Gene | CDH1 | 
| CLNDBN | Hereditary cancer-predisposing syndrome | 
| Reversed | 0 | 
| HGVS | NC_000016.9:g.68772275_68772277delCCCinsT | 
| CLNSRC | |
| CLNACC | RCV000215517.1, | 
