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rs58920878

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common/normal
(C;G) 2 slight (~1.5x) increase in colorectal cancer risk
(G;G) 2 slight (~2x) increase in colorectal cancer risk
ReferenceGRCh38 38.1/141
Chromosome18
Position48923195
GeneSMAD7
is asnp
is mentioned by
dbSNPrs58920878
ebirs58920878
HLIrs58920878
Exacrs58920878
Varsomers58920878
Maprs58920878
PheGenIrs58920878
hapmaprs58920878
1000 genomesrs58920878
hgdprs58920878
ensemblrs58920878
gopubmedrs58920878
geneviewrs58920878
scholarrs58920878
googlers58920878
pharmgkbrs58920878
gwascentralrs58920878
openSNPrs58920878
23andMers58920878
23andMe allrs58920878
SNP Nexus

SNPshotrs58920878
SNPdbers58920878
MSV3drs58920878
GWAS Ctlgrs58920878
GMAF0.343
Max Magnitude2

10.1038/ejhg.2015.72 rs58920878 on 18q21.1 (colorectal cancer OR 1.49, CI: 1.14–1.95, P=0.0035)

[PMID 24448986OA-icon.png] Genome-wide association study identifies a new SMAD7 risk variant associated with colorectal cancer risk in East Asians


[PMID 25375357OA-icon.png] Multiple Functional Risk Variants in a SMAD7 Enhancer Implicate a Colorectal Cancer Risk Haplotype


[PMID 25873010] Clinical relevance of 8q23, 15q13 and 18q21 SNP genotyping to evaluate colorectal cancer risk