Variant: rs1057517764 

    present in Gene: FBXO11;MSH6
    present in Chromosome: 2
    Position on Chromosome: 47805628
    Alleles of this Variant: -/T

rs1057517764 in FBXO11;MSH6 gene and Hereditary Nonpolyposis Colorectal Cancer PMID 20028993 2010 Risks of Lynch syndrome cancers for MSH6 mutation carriers.

rs1057517764 in FBXO11;MSH6 gene and Hereditary Nonpolyposis Colorectal Neoplasms PMID 27064304 2016 Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations.

PMID 24323032 2014 Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing.

rs1057517764 in FBXO11;MSH6 gene and Neoplastic Syndromes, Hereditary PMID 20028993 2010 Risks of Lynch syndrome cancers for MSH6 mutation carriers.

PMID 27064304 2016 Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations.

PMID 24323032 2014 Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing.