rs9929218
| Orientation | plus |
| Stabilized | plus |
| Make rs9929218(A;A) |
| Make rs9929218(A;G) |
| Make rs9929218(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 68787043 |
| Gene | CDH1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9929218 |
| dbSNP (classic) | rs9929218 |
| ClinGen | rs9929218 |
| ebi | rs9929218 |
| HLI | rs9929218 |
| Exac | rs9929218 |
| Gnomad | rs9929218 |
| Varsome | rs9929218 |
| LitVar | rs9929218 |
| Map | rs9929218 |
| PheGenI | rs9929218 |
| Biobank | rs9929218 |
| 1000 genomes | rs9929218 |
| hgdp | rs9929218 |
| ensembl | rs9929218 |
| geneview | rs9929218 |
| scholar | rs9929218 |
| rs9929218 | |
| pharmgkb | rs9929218 |
| gwascentral | rs9929218 |
| openSNP | rs9929218 |
| 23andMe | rs9929218 |
| SNPshot | rs9929218 |
| SNPdbe | rs9929218 |
| MSV3d | rs9929218 |
| GWAS Ctlg | rs9929218 |
| GMAF | 0.2475 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
rs9929218, CDH1; P = 1.2 times 10-8)
| 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 | 1E-8 |
| Odds Ratio | 1.10 [1.06-1.12] |
[PMID 20638935] Susceptibility Genetic Variants Associated With Colorectal Cancer Risk Correlate With Cancer Phenotype
[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 22363440] cis-Expression QTL Analysis of Established Colorectal Cancer Risk Variants in Colon Tumors and Adjacent Normal Tissue
[PMID 18683894] AXIN2 and CDH1 polymorphisms, tooth agenesis, and oral clefts.
[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 23114982] Genome-wide investigation of gene-environment interactions in colorectal cancer
[PMID 23712746] GENETIC SUSCEPTIBILITY VARIANTS ASSOCIATED WITH COLORECTAL CANCER PROGNOSIS
[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 23434150] Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers?
[PMID 24838934] Nucleotide variants of the cancer predisposing gene CDH1 and the risk of non-syndromic cleft lip with or without cleft palate
[PMID 24875374] Variation in the Association Between Colorectal Cancer Susceptibility Loci and Colorectal Polyps by Polyp Type
[PMID 25873087] Analyses of 7,635 patients with colorectal cancer using independent training and validation cohorts show that rs9929218 in CDH1 is a prognostic marker of survival
[PMID 28849422] The more from East-Asian, the better: risk prediction of colorectal cancer risk by GWAS-identified SNPs among Japanese.
