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SNP information rs6687758

RS6687758

Normal allele: AA

Polymorphism rs6687758 is related to topics like this:

Colorectal cancer genes

One of the prevalent cancer syndromes that can be inherited is colon cancer. Chromosome 2 contains...


Research and publications:

  20972440   Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33.

  22076443   Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13.

  22363440   cis-Expression QTL analysis of established colorectal cancer risk variants in colon tumors and adjacent normal tissue.

  22629442   Evaluation of allele-specific somatic changes of genome-wide association study susceptibility alleles in human colorectal cancers.

  22879968   Association of Caucasian-identified variants with colorectal cancer risk in Singapore Chinese.

  22999960   Much of the genetic risk of colorectal cancer is likely to be mediated through susceptibility to adenomas.

  23300701   Genome-wide search for gene-gene interactions in colorectal cancer.

  23350875   A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12.

  23946381   Genetic variants associated with colorectal cancer risk: comprehensive research synopsis, meta-analysis, and epidemiological evidence.

  24373676   Genetic and neuroanatomic associations in sporadic frontotemporal lobar degeneration.

  24764655   Genetic variations in colorectal cancer risk and clinical outcome.

  24801760   Common colorectal cancer risk alleles contribute to the multiple colorectal adenoma phenotype, but do not influence colonic polyposis in FAP.

  24968322   Single nucleotide polymorphisms associated with colorectal cancer susceptibility and loss of heterozygosity in a Taiwanese population.

  24978480   A colorectal cancer susceptibility new variant at 4q26 in the Spanish population identified by genome-wide association analysis.

  24994789   Gene-environment interaction involving recently identified colorectal cancer susceptibility Loci.

  25025429   Single nucleotide polymorphisms with cis-regulatory effects on long non-coding transcripts in human primary monocytes.

  25956580   A colorectal cancer prediction model using traditional and genetic risk scores in Koreans.

  26078566   Association of colorectal cancer susceptibility variants with esophageal cancer in a Chinese population.

  26880076   Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers.

  27146020   Colorectal cancer risk genes are functionally enriched in regulatory pathways.

  27379672   Fine-Mapping of Common Genetic Variants Associated with Colorectal Tumor Risk Identified Potential Functional Variants.

  27424552   Genomics era and complex disorders: Implications of GWAS with special reference to coronary artery disease, type 2 diabetes mellitus, and cancers.

  28084440   Common risk variants for colorectal cancer: an evaluation of associations with age at cancer onset.

  29258461   Effects of interactions between common genetic variants and smoking on colorectal cancer.

  29445242   Colorectal Cancer-Associated Genes Are Associated with Tooth Agenesis and May Have a Role in Tooth Development.

  29464080   Effects of interactions between common genetic variants and alcohol consumption on colorectal cancer risk.

  29547645   Recurrent, low-frequency coding variants contributing to colorectal cancer in the Swedish population.

  29986742   Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility loci.

  31821333   Single nucleotide polymorphisms associated with susceptibility for development of colorectal cancer: Case-control study in a Basque population.

  33153024   Impact of Gene-Environment Interactions on Cancer Development.

  33635380   Latent trait modeling of tau neuropathology in progressive supranuclear palsy.

Gastrointestinal tract cancer

The occurrence of gastrointestinal (GI) tract cancers caused by genetic mutations is widespread...

Hereditary gastric cancer

Gastric cancer is the third leading cause of cancer-related deaths worldwide, with a 5-year...

Pancreas cancer genetic

Up to 15% of pancreatic cancers are attributed to gene mutations that are passed down through...

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