Rs16892766

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is asnp
is mentioned by
dbSNPrs16892766
hapmaprs16892766
hgdprs16892766
ensemblrs16892766
gopubmedrs16892766
scholarrs16892766
googlers16892766
pharmgkbrs16892766
hgvbaseg2prs16892766
medrefsnprs16892766
23andMers16892766
SNP Nexus

Chromosome8
Orientationplus
Position117630683
ReferenceGRCh37 37.1/131
GenotypeEffect
rs16892766(A;A)
rs16892766(A;C)*?
rs16892766(C;C)*?


Genotypes Magnitude Summary
Rs16892766(A;A) 00
? (A;A) (A;C) (C;C) 28
GWAS
SNP rs16892766
PubMedID [PMID 18372905]
Condition Colorectal cancer
Gene EIF3H
Risk Allele A
pValue 3.00E-018
OR 1.27
95% CI 1.20-1.34


Related to COLORECTAL CANCER, SUSCEPTIBILITY TO, 6; CRCS6 according to omim 612231. See also


[PMID 19843678] Enrichment of Low Penetrance Susceptibility Loci in a Dutch Familial Colorectal Cancer Cohort

PharmGKBPA162356770
Name
AnnotationGWAS Results: A genome-wide association study identifies colorectal cancer susceptibility loci on chromosome 10p14 and 8q23.3 (Initial Sample Size: 922 cases, 927 controls; Replication Sample Size: 17,872 cases, 17,526 controls; Risk Allele: rs16892766-A).
Gene-
Featue
EvidencePubMed ID:18372905; Web Resource:http://www.genome.gov/gwastudies/
Drugs
DiseasesColorectal Neoplasms
Curation LevelNon-Curated

[PMID 20638935] Susceptibility Genetic Variants Associated With Colorectal Cancer Risk Correlate With Cancer Phenotype