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