Variant: rs786201042 

    present in Gene: MSH6
    present in Chromosome: 2
    Position on Chromosome: 47783243
    Alleles of this Variant: C/G;T

rs786201042 in MSH6 gene and COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5 PMID 25318681 2015 Characterization of a novel founder MSH6 mutation causing Lynch syndrome in the French Canadian population.

rs786201042 in MSH6 gene and Hereditary Nonpolyposis Colorectal Cancer PMID 25980754 2015 Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.

PMID 20028993 2010 Risks of Lynch syndrome cancers for MSH6 mutation carriers.

PMID 25318681 2015 We identified an MSH6 mutation (c.10C>T, p.Gln4*) causing Lynch syndrome (LS) in 11 French Canadian (FC) families from the Canadian province of Quebec.

rs786201042 in MSH6 gene and Hereditary Nonpolyposis Colorectal Neoplasms PMID 25318681 2015 Characterization of a novel founder MSH6 mutation causing Lynch syndrome in the French Canadian population.

PMID 20028993 2010 Risks of Lynch syndrome cancers for MSH6 mutation carriers.

rs786201042 in MSH6 gene and Neoplastic Syndromes, Hereditary PMID 20028993 2010 Risks of Lynch syndrome cancers for MSH6 mutation carriers.

PMID 28135145 2017 Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer.

PMID 25980754 2015 Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.

PMID 29485237 2018 Recent progress in Lynch syndrome and other familial colorectal cancer syndromes.

PMID 28125075 2017 Assigning clinical meaning to somatic and germ-line whole-exome sequencing data in a prospective cancer precision medicine study.

PMID 25318681 2015 Characterization of a novel founder MSH6 mutation causing Lynch syndrome in the French Canadian population.