rs63749932
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls.
|
9718327 |
1998 |
rs63749932
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Lynch syndrome (hereditary nonpolyposis colorectal cancer) diagnostics.
|
17312306 |
2007 |
rs63749932
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Malignant fibrous histiocytoma is a rare Lynch syndrome-associated tumor in two German families.
|
21598002 |
2011 |
rs63749932
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Genetic testing in hereditary non-polyposis colorectal cancer families with a MSH2, MLH1, or MSH6 mutation.
|
12414824 |
2002 |
rs63749932
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas.
|
11524701 |
2001 |
rs63749932
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Frequent mismatch-repair defects link prostate cancer to Lynch syndrome.
|
27013479 |
2016 |
rs63749932
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Hereditary non-polyposis colorectal cancer (HNPCC): phenotype-genotype correlation between patients with and without identified mutation.
|
12112654 |
2002 |
rs63749932
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
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 |
rs63749932
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Spectrum of germ-line MLH1 and MSH2 mutations in Austrian patients with hereditary nonpolyposis colorectal cancer.
|
15926618 |
2005 |
rs63749932
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Lynch syndrome-associated breast cancers: clinicopathologic characteristics of a case series from the colon cancer family registry.
|
20215533 |
2010 |
rs63749932
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Frequency of mutations in mismatch repair genes in a population-based study of women with ovarian cancer.
|
23047549 |
2012 |
rs63749932
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
The frequency of Muir-Torre syndrome among Lynch syndrome families.
|
18270343 |
2008 |
rs63749932
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Germ-line mutations in mismatch repair genes associated with prostate cancer.
|
19723918 |
2009 |
rs63749932
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers.
|
20587412 |
2010 |
rs63749932
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mutation spectrum in South American Lynch syndrome families.
|
24344984 |
2013 |
rs63749932
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer.
|
15849733 |
2005 |
rs63749932
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Conventional and tissue microarray immunohistochemical expression analysis of mismatch repair in hereditary colorectal tumors.
|
12547705 |
2003 |