rs63750828
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
A
0.800
CausalMutation
CLINVAR
Genetic diagnosis of high-penetrance susceptibility for colorectal cancer (CRC) is achievable for a high proportion of familial CRC by exome sequencing.
25559809
2015
rs63750849
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
25645574
2015
rs63750849
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
25356965
2015
rs63750849
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.
25394175
2015
rs63750849
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines.
25452455
2015
rs63750849
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Lynch Syndrome: A Primer for Urologists and Panel Recommendations.
25711197
2015
rs63750875
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
25356965
2015
rs63750875
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Lynch Syndrome: A Primer for Urologists and Panel Recommendations.
25711197
2015
rs63750875
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines.
25452455
2015
rs63750875
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
25645574
2015
rs63750875
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.
25394175
2015
rs63751207
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines.
25452455
2015
rs63751207
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
25356965
2015
rs63751207
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Lynch Syndrome: A Primer for Urologists and Panel Recommendations.
25711197
2015
rs63751207
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
25645574
2015
rs28929483
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.
24493721
2014
rs28929483
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-society Task Force on colorectal cancer.
25070057
2014
rs28929483
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
ACMG technical standards and guidelines for genetic testing for inherited colorectal cancer (Lynch syndrome, familial adenomatous polyposis, and MYH-associated polyposis).
24310308
2014
rs28929483
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-Society Task Force on Colorectal Cancer.
25003300
2014
rs28929484
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
ACMG technical standards and guidelines for genetic testing for inherited colorectal cancer (Lynch syndrome, familial adenomatous polyposis, and MYH-associated polyposis).
24310308
2014
rs28929484
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-Society Task Force on Colorectal Cancer.
25003300
2014
rs28929484
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-society Task Force on colorectal cancer.
25070057
2014
rs28929484
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.
24493721
2014
rs587779067
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
G
0.800
GeneticVariation
CLINVAR
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.
24362816
2014
rs587779067
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-Society Task Force on Colorectal Cancer.
25003300
2014