×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
0.110
GeneticVariation
group
CLINVAR
Dominant effects of an Msh6 missense mutation on DNA repair and cancer susceptibility.
15324697
2004
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
0.110
GeneticVariation
group
CLINVAR
MSH6 missense mutations are often associated with no or low cancer susceptibility.
15354210
2004
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
0.110
CausalMutation
group
CLINVAR
Germline mutations in MLH1, MSH2 and MSH6 in Korean hereditary non-polyposis colorectal cancer families.
15365995
2004
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
0.110
GeneticVariation
group
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
0.110
CausalMutation
group
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
0.110
CausalMutation
group
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
0.110
CausalMutation
group
CLINVAR
Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).
15872200
2005
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
0.110
CausalMutation
group
CLINVAR
Immunohistochemistry identifies carriers of mismatch repair gene defects causing hereditary nonpolyposis colorectal cancer.
16034045
2005
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
0.110
GeneticVariation
group
CLINVAR
High frequency of hereditary colorectal cancer in Newfoundland likely involves novel susceptibility genes.
16203774
2005
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
0.110
CausalMutation
group
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
0.110
CausalMutation
group
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
0.110
CausalMutation
group
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
0.110
GeneticVariation
group
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
0.110
GeneticVariation
group
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
0.110
CausalMutation
group
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
0.110
CausalMutation
group
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
0.110
CausalMutation
group
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
0.110
GeneticVariation
group
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
0.110
GeneticVariation
group
CLINVAR
Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients.
16885385
2006
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
0.110
CausalMutation
group
CLINVAR
Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients.
16885385
2006
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
0.110
CausalMutation
group
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
0.110
CausalMutation
group
CLINVAR
MSH6 mutation in Muir-Torre syndrome: could this be a rare finding?
17199584
2007
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
0.110
GeneticVariation
group
CLINVAR
Lynch syndrome (hereditary nonpolyposis colorectal cancer) diagnostics.
17312306
2007
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
0.110
CausalMutation
group
CLINVAR
An individual with Muir-Torre syndrome found to have a pathogenic MSH6 gene mutation.
17323113
2007
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
0.110
CausalMutation
group
CLINVAR
Patients with an unexplained microsatellite instable tumour have a low risk of familial cancer.
17453009
2007