Variant: rs193922343 

    present in Gene: FBXO11;MSH6
    present in Chromosome: 2
    Position on Chromosome: 47806254
    Alleles of this Variant: AGAA/-;AGAAAAGAA;AGAAAGAA

rs193922343 in FBXO11;MSH6 gene and COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5 PMID 21642682 2011 Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.

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

PMID 18389388 2008 Mutation spectrum in HNPCC in the Israeli population.

rs193922343 in FBXO11;MSH6 gene and Hereditary Nonpolyposis Colorectal Cancer PMID 24689082 2014 A massive parallel sequencing workflow for diagnostic genetic testing of mismatch repair genes.

rs193922343 in FBXO11;MSH6 gene and Hereditary Nonpolyposis Colorectal Neoplasms PMID 24689082 2014 A massive parallel sequencing workflow for diagnostic genetic testing of mismatch repair genes.

PMID 21642682 2011 Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.

PMID 18389388 2008 Mutation spectrum in HNPCC in the Israeli population.

rs193922343 in FBXO11;MSH6 gene and Neoplastic Syndromes, Hereditary PMID 21642682 2011 Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.

PMID 24689082 2014 A massive parallel sequencing workflow for diagnostic genetic testing of mismatch repair genes.