rs55778204
|
|
|
0.700 |
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 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Population-based molecular detection of hereditary nonpolyposis colorectal cancer.
|
10829038 |
2000 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility.
|
20065170 |
2010 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Functional analysis of HNPCC-related missense mutations in MSH2.
|
18822302 |
2008 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutational analysis of the hMSH2 gene reveals a three base pair deletion in a family predisposed to colorectal cancer development.
|
7874129 |
1994 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
MSH2 missense mutations and HNPCC syndrome: pathogenicity assessment in a human expression system.
|
18781619 |
2008 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Lynch Syndrome: A Primer for Urologists and Panel Recommendations.
|
25711197 |
2015 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Hereditary nonpolyposis colorectal cancer: pitfalls in deletion screening in MSH2 and MLH1 genes.
|
15870828 |
2005 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Practice parameters for the identification and testing of patients at risk for dominantly inherited colorectal cancer--supporting documentation.
|
11598466 |
2001 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
|
27854360 |
2017 |
rs55778204
|
|
|
0.700 |
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 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
A novel missense germline mutation in exon 2 of the hMSH2 gene in a HNPCC family from Southern Italy.
|
15896463 |
2005 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Functional analysis of human MutSalpha and MutSbeta complexes in yeast.
|
9889267 |
1999 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Identification of concurrent germ-line mutations in hMSH2 and/or hMLH1 in Japanese hereditary nonpolyposis colorectal cancer kindreds.
|
9419403 |
1997 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene.
|
12658575 |
2003 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Assessment of pathogenicity criteria for constitutional missense mutations of the hereditary nonpolyposis colorectal cancer genes MLH1 and MSH2.
|
10573010 |
2000 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants.
|
22102614 |
2012 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
|
25356965 |
2015 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Gene symbol: hMSH2. Disease: Hereditary nonpolyposis colorectal cancer.
|
15046096 |
2004 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
|
23788249 |
2013 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
HNPCC mutations in hMSH2 result in reduced hMSH2-hMSH6 molecular switch functions.
|
12124176 |
2002 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Identification of individuals at risk for Lynch syndrome using targeted evaluations and genetic testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer joint practice guideline.
|
22167527 |
2012 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
|
25645574 |
2015 |
rs55778204
|
|
|
0.700 |
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 |
rs55778204
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Informing family members of individuals with Lynch syndrome: a guideline for clinical geneticists.
|
23535968 |
2013 |