rs3824999
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3824999(A;A) |
| Make rs3824999(A;C) |
| Make rs3824999(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 74634505 |
| Gene | POLD3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3824999 |
| dbSNP (classic) | rs3824999 |
| ClinGen | rs3824999 |
| ebi | rs3824999 |
| HLI | rs3824999 |
| Exac | rs3824999 |
| Gnomad | rs3824999 |
| Varsome | rs3824999 |
| LitVar | rs3824999 |
| Map | rs3824999 |
| PheGenI | rs3824999 |
| Biobank | rs3824999 |
| 1000 genomes | rs3824999 |
| hgdp | rs3824999 |
| ensembl | rs3824999 |
| geneview | rs3824999 |
| scholar | rs3824999 |
| rs3824999 | |
| pharmgkb | rs3824999 |
| gwascentral | rs3824999 |
| openSNP | rs3824999 |
| 23andMe | rs3824999 |
| SNPshot | rs3824999 |
| SNPdbe | rs3824999 |
| MSV3d | rs3824999 |
| GWAS Ctlg | rs3824999 |
| GMAF | 0.3825 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22634755 ]
|
| Trait | |
| Title | Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk. |
| Risk Allele | |
| P-val | 4E-10 |
| Odds Ratio | 1.0800 None |
[PMID 24978480] A Colorectal Cancer Susceptibility New Variant at 4q26 in the Spanish Population Identified by Genome-Wide Association Analysis
