rs78897872
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs78897872(A;A) |
| Make rs78897872(A;C) |
| Make rs78897872(C;C) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 5 |
| Position | 112834387 |
| Gene | APC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs78897872 |
| dbSNP (classic) | rs78897872 |
| ClinGen | rs78897872 |
| ebi | rs78897872 |
| HLI | rs78897872 |
| Exac | rs78897872 |
| Gnomad | rs78897872 |
| Varsome | rs78897872 |
| LitVar | rs78897872 |
| Map | rs78897872 |
| PheGenI | rs78897872 |
| Biobank | rs78897872 |
| 1000 genomes | rs78897872 |
| hgdp | rs78897872 |
| ensembl | rs78897872 |
| geneview | rs78897872 |
| scholar | rs78897872 |
| rs78897872 | |
| pharmgkb | rs78897872 |
| gwascentral | rs78897872 |
| openSNP | rs78897872 |
| 23andMe | rs78897872 |
| SNPshot | rs78897872 |
| SNPdbe | rs78897872 |
| MSV3d | rs78897872 |
| GWAS Ctlg | rs78897872 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs78897872(C;C) |
| Alt | rs78897872(C;C) |
| Reference | rs78897872(A;A) |
| Significance | Other |
| Disease | Familial colorectal cancer |
| Variation | info |
| Gene | APC |
| CLNDBN | Familial colorectal cancer |
| Reversed | 0 |
| HGVS | NC_000005.9:g.112170084A>C |
| CLNSRC | |
| CLNACC | RCV000074195.1, |
