rs980578884
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs980578884(A;A) |
| Make rs980578884(A;G) |
| Make rs980578884(G;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 12 |
| Position | 132673217 |
| Gene | POLE |
| is a | snp |
| is | mentioned by |
| dbSNP | rs980578884 |
| dbSNP (classic) | rs980578884 |
| ClinGen | rs980578884 |
| ebi | rs980578884 |
| HLI | rs980578884 |
| Exac | rs980578884 |
| Gnomad | rs980578884 |
| Varsome | rs980578884 |
| LitVar | rs980578884 |
| Map | rs980578884 |
| PheGenI | rs980578884 |
| Biobank | rs980578884 |
| 1000 genomes | rs980578884 |
| hgdp | rs980578884 |
| ensembl | rs980578884 |
| geneview | rs980578884 |
| scholar | rs980578884 |
| rs980578884 | |
| pharmgkb | rs980578884 |
| gwascentral | rs980578884 |
| openSNP | rs980578884 |
| 23andMe | rs980578884 |
| SNPshot | rs980578884 |
| SNPdbe | rs980578884 |
| MSV3d | rs980578884 |
| GWAS Ctlg | rs980578884 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs980578884(T;T) |
| Alt | rs980578884(T;T) |
| Reference | Rs980578884(C;C) |
| Significance | Pathogenic |
| Disease | Colorectal cancer |
| Variation | info |
| Gene | POLE |
| CLNDBN | Colorectal cancer, susceptibility to, 12 |
| Reversed | 0 |
| HGVS | NC_000012.11:g.133249803C>T |
| CLNSRC | |
| CLNACC | RCV000417197.1, |
