rs63750828
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Thyroid cancer in a patient with Lynch syndrome - case report and literature review.
|
28769567 |
2017 |
rs63750828
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
rs63750828
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Oligonucleotide-directed mutagenesis screen to identify pathogenic Lynch syndrome-associated MSH2 DNA mismatch repair gene variants.
|
26951660 |
2016 |
rs63750828
|
|
A |
0.700 |
GeneticVariation |
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 |
rs63750828
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
UMD-MLH1/MSH2/MSH6 databases: description and analysis of genetic variations in French Lynch syndrome families.
|
23729658 |
2013 |
rs63750828
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.
|
21642682 |
2011 |
rs63750828
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Mechanisms of pathogenicity in human MSH2 missense mutants.
|
18951462 |
2008 |
rs63750828
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Functional characterization of pathogenic human MSH2 missense mutations in Saccharomyces cerevisiae.
|
17720936 |
2007 |
rs63750828
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Pathogenicity of MSH2 missense mutations is typically associated with impaired repair capability of the mutated protein.
|
17101317 |
2006 |
rs63750828
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer.
|
15849733 |
2005 |
rs63750828
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Routine testing for mismatch repair deficiency in sporadic colorectal cancer is justified.
|
16175654 |
2005 |
rs63750828
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Cancer risk in 348 French MSH2 or MLH1 gene carriers.
|
12624141 |
2003 |