rs587779001
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Comprehensive analysis of the MLH1 promoter region in 480 patients with colorectal cancer and 1150 controls reveals new variants including one with a heritable constitutional MLH1 epimutation.
|
29472279 |
2018 |
rs63751221
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Clinical and Genetic Implications of DNA Mismatch Repair Deficiency in Biliary Tract Cancers Associated with Lynch Syndrome.
|
29238914 |
2018 |
rs267607732
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Spectrum of mismatch repair gene mutations and clinical presentation of Hispanic individuals with Lynch syndrome.
|
28449805 |
2017 |
rs267607898
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Multigene Panel Testing Provides a New Perspective on Lynch Syndrome.
|
28514183 |
2017 |
rs267607901
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Pancreatic Cancer in Lynch Syndrome Patients.
|
29151953 |
2017 |
rs63749986
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Hereditary cancer syndromes in Latino populations: genetic characterization and surveillance guidelines.
|
28127413 |
2017 |
rs63750217
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Spectrum of mismatch repair gene mutations and clinical presentation of Hispanic individuals with Lynch syndrome.
|
28449805 |
2017 |
rs63750217
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Assessment of the InSiGHT Interpretation Criteria for the Clinical Classification of 24 MLH1 and MSH2 Gene Variants.
|
27629256 |
2017 |
rs63750217
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America.
|
28874130 |
2017 |
rs63750217
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
New EPCAM founder deletion in Polish population.
|
28369810 |
2017 |
rs63750540
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.
|
27978560 |
2017 |
rs63751194
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A molecular inversion probe-based next-generation sequencing panel to detect germline mutations in Chinese early-onset colorectal cancer patients.
|
28445943 |
2017 |
rs63751310
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America.
|
28874130 |
2017 |
rs63751310
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Germline Mutations in Cancer Susceptibility Genes in a Large Series of Unselected Breast Cancer Patients.
|
28724667 |
2017 |
rs63751592
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer.
|
28135145 |
2017 |
rs63751615
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Multigene Panel Testing Provides a New Perspective on Lynch Syndrome.
|
28514183 |
2017 |
rs63751615
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A molecular inversion probe-based next-generation sequencing panel to detect germline mutations in Chinese early-onset colorectal cancer patients.
|
28445943 |
2017 |
rs63751711
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Hereditary cancer syndromes in Latino populations: genetic characterization and surveillance guidelines.
|
28127413 |
2017 |
rs878853785
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Spectrum of mismatch repair gene mutations and clinical presentation of Hispanic individuals with Lynch syndrome.
|
28449805 |
2017 |
rs267607720
|
|
G |
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 |
rs267607749
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
|
27601186 |
2016 |
rs267607767
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
rs267607780
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Germline mutations in PMS2 and MLH1 in individuals with solitary loss of PMS2 expression in colorectal carcinomas from the Colon Cancer Family Registry Cohort.
|
26895986 |
2016 |
rs267607789
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Germline mutations in PMS2 and MLH1 in individuals with solitary loss of PMS2 expression in colorectal carcinomas from the Colon Cancer Family Registry Cohort.
|
26895986 |
2016 |
rs267607794
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |