rs79630786
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs79630786(C;C) |
| Make rs79630786(C;G) |
| Make rs79630786(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 5 |
| Position | 112843107 |
| Gene | APC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs79630786 |
| dbSNP (classic) | rs79630786 |
| ClinGen | rs79630786 |
| ebi | rs79630786 |
| HLI | rs79630786 |
| Exac | rs79630786 |
| Gnomad | rs79630786 |
| Varsome | rs79630786 |
| LitVar | rs79630786 |
| Map | rs79630786 |
| PheGenI | rs79630786 |
| Biobank | rs79630786 |
| 1000 genomes | rs79630786 |
| hgdp | rs79630786 |
| ensembl | rs79630786 |
| geneview | rs79630786 |
| scholar | rs79630786 |
| rs79630786 | |
| pharmgkb | rs79630786 |
| gwascentral | rs79630786 |
| openSNP | rs79630786 |
| 23andMe | rs79630786 |
| SNPshot | rs79630786 |
| SNPdbe | rs79630786 |
| MSV3d | rs79630786 |
| GWAS Ctlg | rs79630786 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs79630786(G;G) |
| Alt | rs79630786(G;G) |
| Reference | rs79630786(C;C) |
| Significance | Other |
| Disease | Familial colorectal cancer |
| Variation | info |
| Gene | APC |
| CLNDBN | Familial colorectal cancer |
| Reversed | 0 |
| HGVS | NC_000005.9:g.112178804C>G |
| CLNSRC | |
| CLNACC | RCV000073624.1, |
