rs786202351
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs786202351(G;G) |
| Make rs786202351(G;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 5 |
| Position | 112780905 |
| Gene | APC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs786202351 |
| dbSNP (classic) | rs786202351 |
| ClinGen | rs786202351 |
| ebi | rs786202351 |
| HLI | rs786202351 |
| Exac | rs786202351 |
| Gnomad | rs786202351 |
| Varsome | rs786202351 |
| LitVar | rs786202351 |
| Map | rs786202351 |
| PheGenI | rs786202351 |
| Biobank | rs786202351 |
| 1000 genomes | rs786202351 |
| hgdp | rs786202351 |
| ensembl | rs786202351 |
| geneview | rs786202351 |
| scholar | rs786202351 |
| rs786202351 | |
| pharmgkb | rs786202351 |
| gwascentral | rs786202351 |
| openSNP | rs786202351 |
| 23andMe | rs786202351 |
| SNPshot | rs786202351 |
| SNPdbe | rs786202351 |
| MSV3d | rs786202351 |
| GWAS Ctlg | rs786202351 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs786202351(G;G) |
| Alt | rs786202351(G;G) |
| Reference | Rs786202351(T;T) |
| Significance | Probable-Pathogenic |
| Disease | Hereditary cancer-predisposing syndrome |
| Variation | info |
| Gene | APC |
| CLNDBN | Hereditary cancer-predisposing syndrome |
| Reversed | 0 |
| HGVS | NC_000005.9:g.112116602T>G |
| CLNSRC | |
| CLNACC | RCV000165115.1, |
