rs139075637
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;T) | 1 | Variant of uncertain significance wrt colon cancer; could be benign |
| Make rs139075637(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 12 |
| Position | 132676594 |
| Gene | POLE |
| is a | snp |
| is | mentioned by |
| dbSNP | rs139075637 |
| dbSNP (classic) | rs139075637 |
| ClinGen | rs139075637 |
| ebi | rs139075637 |
| HLI | rs139075637 |
| Exac | rs139075637 |
| Gnomad | rs139075637 |
| Varsome | rs139075637 |
| LitVar | rs139075637 |
| Map | rs139075637 |
| PheGenI | rs139075637 |
| Biobank | rs139075637 |
| 1000 genomes | rs139075637 |
| hgdp | rs139075637 |
| ensembl | rs139075637 |
| geneview | rs139075637 |
| scholar | rs139075637 |
| rs139075637 | |
| pharmgkb | rs139075637 |
| gwascentral | rs139075637 |
| openSNP | rs139075637 |
| 23andMe | rs139075637 |
| SNPshot | rs139075637 |
| SNPdbe | rs139075637 |
| MSV3d | rs139075637 |
| GWAS Ctlg | rs139075637 |
| Max Magnitude | 1 |
aka c.861T>A, p.Asp287Glu
As of 2018, the minor allele for this SNP is considered to be either likely to be benign or of uncertain significance by the majority of submitters to ClinVar.
