Variant: rs587783056 

    present in Gene: MSH6;FBXO11
    present in Chromosome: 2
    Position on Chromosome: 47799685
    Alleles of this Variant: TT/-

rs587783056 in MSH6;FBXO11 gene and Colorectal cancer, hereditary nonpolyposis, type 1 PMID 20028993 2010 Risks of Lynch syndrome cancers for MSH6 mutation carriers.

PMID 24362816 2014 Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.

rs587783056 in MSH6;FBXO11 gene and Hereditary Nonpolyposis Colorectal Cancer PMID 26023681 2015 Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic.

rs587783056 in MSH6;FBXO11 gene and Hereditary Nonpolyposis Colorectal Neoplasms PMID 26023681 2015 Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic.

rs587783056 in MSH6;FBXO11 gene and Neoplastic Syndromes, Hereditary PMID 26023681 2015 Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic.