rs786201856
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs786201856(C;T) |
| Make rs786201856(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 5 |
| Position | 112815507 |
| Gene | APC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs786201856 |
| dbSNP (classic) | rs786201856 |
| ClinGen | rs786201856 |
| ebi | rs786201856 |
| HLI | rs786201856 |
| Exac | rs786201856 |
| Gnomad | rs786201856 |
| Varsome | rs786201856 |
| LitVar | rs786201856 |
| Map | rs786201856 |
| PheGenI | rs786201856 |
| Biobank | rs786201856 |
| 1000 genomes | rs786201856 |
| hgdp | rs786201856 |
| ensembl | rs786201856 |
| geneview | rs786201856 |
| scholar | rs786201856 |
| rs786201856 | |
| pharmgkb | rs786201856 |
| gwascentral | rs786201856 |
| openSNP | rs786201856 |
| 23andMe | rs786201856 |
| SNPshot | rs786201856 |
| SNPdbe | rs786201856 |
| MSV3d | rs786201856 |
| GWAS Ctlg | rs786201856 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs786201856(T;T) |
| Alt | rs786201856(T;T) |
| Reference | Rs786201856(C;C) |
| Significance | Pathogenic |
| Disease | Hereditary cancer-predisposing syndrome not provided Familial adenomatous polyposis 1 |
| Variation | info |
| Gene | APC |
| CLNDBN | Hereditary cancer-predisposing syndrome not provided Familial adenomatous polyposis 1 |
| Reversed | 0 |
| HGVS | NC_000005.9:g.112151204C>T |
| CLNSRC | |
| CLNACC | RCV000164351.2, RCV000202113.1, RCV000226000.2, |
