rs4813802
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4813802(G;G) |
| Make rs4813802(G;T) |
| Make rs4813802(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 6718948 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4813802 |
| dbSNP (classic) | rs4813802 |
| ClinGen | rs4813802 |
| ebi | rs4813802 |
| HLI | rs4813802 |
| Exac | rs4813802 |
| Gnomad | rs4813802 |
| Varsome | rs4813802 |
| LitVar | rs4813802 |
| Map | rs4813802 |
| PheGenI | rs4813802 |
| Biobank | rs4813802 |
| 1000 genomes | rs4813802 |
| hgdp | rs4813802 |
| ensembl | rs4813802 |
| geneview | rs4813802 |
| scholar | rs4813802 |
| rs4813802 | |
| pharmgkb | rs4813802 |
| gwascentral | rs4813802 |
| openSNP | rs4813802 |
| 23andMe | rs4813802 |
| SNPshot | rs4813802 |
| SNPdbe | rs4813802 |
| MSV3d | rs4813802 |
| GWAS Ctlg | rs4813802 |
| GMAF | 0.2548 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21655089
] Multiple Common Susceptibility Variants near BMP Pathway Loci GREM1, BMP4, and BMP2 Explain Part of the Missing Heritability of Colorectal Cancer
[PMID 21761138
] Meta-analysis of new genome-wide association studies of colorectal cancer risk
[PMID 22045029] Relationship between 16 susceptibility loci and colorectal cancer phenotype in 3146 patients.
| GWAS snp | |
|---|---|
| PMID | [PMID 23266556 |
| Trait | Colorectal cancer |
| Title | Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-wide Meta-analysis. |
| Risk Allele | G |
| P-val | 7E-6 |
| Odds Ratio | 1.10 [1.05-1.14] |
[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.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 20
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip Ancestry v2c
- On chip Ancestry v2d
