The genetic variant on chromosome 10p14 is associated with risk of colorectal cancer: results from a case-control study and a meta-analysis.

doi:10.1371/journal.pone.0064310

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

The genetic variant on chromosome 10p14 is associated with risk of colorectal cancer: results from a case-control study and a meta-analysis.

PloS one - 1 Jan 2013

Qin Qin, Liu Li, Zhong Rong, Zou Li, Yin Jieyun, Zhu Beibei, Cao Beibei, Chen Wei, Chen Jigui, Li Xiaorong, Li Tingting, Lu Xuzai, Lou Jiao, Ke Juntao, Wei Sheng, Miao Xiaoping, Nie Shaofa

Abstract excerpt

BACKGROUND: A common single nucleotide polymorphism (SNP), rs10795668, located at 10p14, was first identified to be significantly associated with risk of colorectal cancer (CRC) by a genome-wide association study (GWAS) in 2008; however, another GWAS and following replication studies yielded conflicting results. METHODS: We conducted a case-control study of 470 cases and 475 controls in a Chinese population and...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Case-Control Studies

Share to China

Share to Chromosomes, Human, Pair 10

Share to Colorectal Neoplasms

Share to Genetic Heterogeneity

Share to Genetic Predisposition to Disease

Share to Polymorphism, Single Nucleotide

Source

Open in PubMed Open full text

Identifiers

PMID: 23717594
DOI: 10.1371/journal.pone.0064310
PMCID: PMC3661459

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The genetic variant on chromosome 10p14 is associated with risk of colorectal cancer: results from a case-control study and a meta-analysis.PMID 23717594Read ↗

A comprehensive meta-analysis of genetic associations between five key SNPs and colorectal cancer risk.Semantic proximity Read ↗

Japanese genome-wide association study identifies a significant colorectal cancer susceptibility locus at chromosome 10p14.Semantic proximity Read ↗

Risk of genome-wide association study-identified genetic variants for colorectal cancer in a Chinese population.Semantic proximity Read ↗

The SNP rs961253 in 20p12.3 is associated with colorectal cancer risk: a case-control study and a meta-analysis of the published literature.Semantic proximity Read ↗

Genetic variants identified by GWAS was associated with colorectal cancer in the Han Chinese population.Semantic proximity Read ↗

Multiple genetic variants are associated with colorectal cancer risk in the Han Chinese population.Semantic proximity Read ↗

Analyzing large-scale samples confirms the association between rs16892766 polymorphism and colorectal cancer susceptibility.Semantic proximity Read ↗

SMAD7 gene polymorphisms and their influence on patients with colorectal cancer.Semantic proximity Read ↗

rs719725 Polymorphism and Colorectal Cancer Susceptibility: A Meta-analysis.Semantic proximity Read ↗

Colorectal cancer-susceptibility single-nucleotide polymorphisms in Korean population.Semantic proximity Read ↗

A novel SNP in promoter region of RP11-3N2.1 is associated with reduced risk of colorectal cancer.Semantic proximity Read ↗

A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.