rs961253
| Orientation | plus |
| Stabilized | plus |
| Make rs961253(A;A) |
| Make rs961253(A;C) |
| Make rs961253(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 6423634 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs961253 |
| dbSNP (classic) | rs961253 |
| ClinGen | rs961253 |
| ebi | rs961253 |
| HLI | rs961253 |
| Exac | rs961253 |
| Gnomad | rs961253 |
| Varsome | rs961253 |
| LitVar | rs961253 |
| Map | rs961253 |
| PheGenI | rs961253 |
| Biobank | rs961253 |
| 1000 genomes | rs961253 |
| hgdp | rs961253 |
| ensembl | rs961253 |
| geneview | rs961253 |
| scholar | rs961253 |
| rs961253 | |
| pharmgkb | rs961253 |
| gwascentral | rs961253 |
| openSNP | rs961253 |
| 23andMe | rs961253 |
| SNPshot | rs961253 |
| SNPdbe | rs961253 |
| MSV3d | rs961253 |
| GWAS Ctlg | rs961253 |
| GMAF | 0.2874 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
nature colorectal cancer rs961253; P = 2.0 times 10-10
| GWAS snp | |
|---|---|
| PMID | [PMID 19011631 ]
|
| Trait | Colorectal cancer |
| Title | Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer |
| Risk Allele | A |
| P-val | 2E-10 |
| Odds Ratio | 1.12 [1.08-1.16] |
[PMID 20530476] Risk of Genome-Wide Association Study-Identified Genetic Variants for Colorectal Cancer in a Chinese Population
[PMID 21119214] Colorectal Cancer Susceptibility Loci in a Population-Based Study: Associations with Morphological Parameters
[PMID 22367214] Characterization of gene-environment interactions for colorectal cancer susceptibility loci
[PMID 22505654] GWAS-identified colorectal cancer susceptibility loci associated with clinical outcomes
[PMID 22509336] The SNP rs961253 in 20p12.3 Is Associated with Colorectal Cancer Risk: A Case-Control Study and a Meta-Analysis of the Published Literature
[PMID 19639606] Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.
[PMID 20501757] Low-penetrance susceptibility variants in familial colorectal cancer.
[PMID 20648012] Association studies on 11 published colorectal cancer risk loci.
[PMID 21071539] Generalizability and epidemiologic characterization of eleven colorectal cancer GWAS hits in multiple populations.
[PMID 21314996] Systematic search for enhancer elements and somatic allelic imbalance at seven low-penetrance colorectal cancer predisposition loci.
[PMID 22045029] Relationship between 16 susceptibility loci and colorectal cancer phenotype in 3146 patients.
[PMID 22235025] Susceptibility genetic variants associated with early-onset colorectal cancer.
[PMID 23359760] Single-nucleotide polymorphism associations for colorectal cancer in southern chinese population
[PMID 23537995] Evidence of Colorectal Cancer Risk Associated Variant Lys25Ser in the proximity of Human Bone Morphogenetic Protein 2
[PMID 22848671] Association of eleven common, low-penetrance colorectal cancer susceptibility genetic variants at six risk loci with clinical outcome.
[PMID 22999960] Much of the genetic risk of colorectal cancer is likely to be mediated through susceptibility to adenomas.
[PMID 23161572] BMP2/BMP4 colorectal cancer susceptibility loci in northern and southern European populations.
[PMID 23434150] Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers?
[PMID 24875374] Variation in the Association Between Colorectal Cancer Susceptibility Loci and Colorectal Polyps by Polyp Type
[PMID 32928932] Genetic Colorectal Cancer and Adenoma Risk Variants are Associated with Increasing Adenoma Counts.
