×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German Hereditary Nonpolyposis Colorectal Cancer Consortium.
15483016 2004
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Penetrance and expressivity of MSH6 germline mutations in seven kindreds not ascertained by family history.
15098177 2004
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: a population-based study in northern Sweden.
14961575 2004
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German Hereditary Nonpolyposis Colorectal Cancer Consortium.
15483016 2004
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance.
15236168 2004
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Two Swedish founder MSH6 mutations, one nonsense and one missense, conferring high cumulative risk of Lynch syndrome.
16283884 2005
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
High frequency of hereditary colorectal cancer in Newfoundland likely involves novel susceptibility genes.
16203774 2005
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Immunohistochemistry identifies carriers of mismatch repair gene defects causing hereditary nonpolyposis colorectal cancer.
16034045 2005
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Molecular analysis of familial endometrial carcinoma: a manifestation of hereditary nonpolyposis colorectal cancer or a separate syndrome?
15837969 2005
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).
15872200 2005
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients.
16885385 2006
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Frequency and nature of hMSH6 germline mutations in Polish patients with colorectal, endometrial and ovarian cancers.
16813607 2006
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Germline mutations of the hMLH1 and hMSH2 mismatch repair genes in Belgian hereditary nonpolyposis colon cancer (HNPCC) patients.
16736289 2006
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients.
16885385 2006
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Compound heterozygosity for two MSH6 mutations in a patient with early onset of HNPCC-associated cancers, but without hematological malignancy and brain tumor.
16418736 2006
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer.
16807412 2006
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Very low prevalence of germline MSH6 mutations in hereditary non-polyposis colorectal cancer suspected patients with colorectal cancer without microsatellite instability.
17117178 2006
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Polyposis and early cancer in a patient with low penetrant mutations in MSH6 and APC: hereditary colorectal cancer as a polygenic trait.
16525781 2006
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Cancer risks for mismatch repair gene mutation carriers: a population-based early onset case-family study.
16616355 2006
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
The contribution of the hereditary nonpolyposis colorectal cancer syndrome to the development of ovarian cancer.
16360201 2006
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Compound heterozygosity for two MSH6 mutations in a patient with early onset of HNPCC-associated cancers, but without hematological malignancy and brain tumor.
16418736 2006
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Structure of the human MutSalpha DNA lesion recognition complex.
17531815 2007
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Patients with an unexplained microsatellite instable tumour have a low risk of familial cancer.
17453009 2007
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
MSH6 mutation in Muir-Torre syndrome: could this be a rare finding?
17199584 2007
×
Entrez Id: 2956
Gene Symbol: MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Nine novel pathogenic germline mutations in MLH1, MSH2, MSH6 and PMS2 in families with Lynch syndrome.
17653898 2007