Variant: rs1553408388 

    present in Gene: MSH6
    present in Chromosome: 2
    Position on Chromosome: 47783453
    Alleles of this Variant: G/T

rs1553408388 in MSH6 gene and Hereditary Nonpolyposis Colorectal Neoplasms PMID 20028993 2010 Risks of Lynch syndrome cancers for MSH6 mutation carriers.

PMID 16885385 2006 Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients.

PMID 17909073 2007 Comment on: Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients.

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

rs1553408388 in MSH6 gene and Neoplastic Syndromes, Hereditary PMID 20028993 2010 Risks of Lynch syndrome cancers for MSH6 mutation carriers.

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

PMID 17909073 2007 Comment on: Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients.

PMID 16885385 2006 Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients.