rs786201042
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Recent progress in Lynch syndrome and other familial colorectal cancer syndromes.
|
29485237 |
2018 |
rs1316409501
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity.
|
28531214 |
2017 |
rs146816935
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Loss of MSH2 and MSH6 due to heterozygous germline defects in MSH3 and MSH6.
|
28528517 |
2017 |
rs267608042
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Spectrum of mismatch repair gene mutations and clinical presentation of Hispanic individuals with Lynch syndrome.
|
28449805 |
2017 |
rs267608042
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America.
|
28874130 |
2017 |
rs267608078
|
|
AC |
0.700 |
CausalMutation |
CLINVAR |
Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome.
|
28481244 |
2017 |
rs267608083
|
|
CA |
0.700 |
CausalMutation |
CLINVAR |
Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome.
|
28195393 |
2017 |
rs267608083
|
|
CA |
0.700 |
CausalMutation |
CLINVAR |
Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes.
|
28944238 |
2017 |
rs398123231
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Improving Mutation Screening in Patients with Colorectal Cancer Predisposition Using Next-Generation Sequencing.
|
28502729 |
2017 |
rs587779204
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Clinical Challenges Associated with Universal Screening for Lynch Syndrome-Associated Endometrial Cancer.
|
27965287 |
2017 |
rs587779204
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.
|
27978560 |
2017 |
rs587779227
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes.
|
28944238 |
2017 |
rs587779227
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity.
|
28531214 |
2017 |
rs587779255
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Prevalence of pathogenic germline variants detected by multigene sequencing in unselected Japanese patients with ovarian cancer.
|
29348823 |
2017 |
rs587781462
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Longitudinal analysis of treatment-induced genomic alterations in gliomas.
|
28153049 |
2017 |
rs587781544
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Loss of MSH2 and MSH6 due to heterozygous germline defects in MSH3 and MSH6.
|
28528517 |
2017 |
rs587782111
|
|
TA |
0.700 |
CausalMutation |
CLINVAR |
Improving Mutation Screening in Patients with Colorectal Cancer Predisposition Using Next-Generation Sequencing.
|
28502729 |
2017 |
rs63749874
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Lower gastrointestinal neuroendocrine neoplasms associated with hereditary cancer syndromes: a case series.
|
28283864 |
2017 |
rs63750019
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes.
|
28944238 |
2017 |
rs63750617
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing.
|
27696107 |
2017 |
rs63750617
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome.
|
28481244 |
2017 |
rs63750909
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A rare case of choroid plexus carcinoma that led to the diagnosis of Lynch syndrome (hereditary nonpolyposis colorectal cancer).
|
28460341 |
2017 |
rs63751017
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Correlation between germline mutations in MMR genes and microsatellite instability in ovarian cancer specimens.
|
28176205 |
2017 |
rs63751017
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Targeted sequencing of established and candidate colorectal cancer genes in the Colon Cancer Family Registry Cohort.
|
29212164 |
2017 |
rs63751327
|
|
TA |
0.700 |
CausalMutation |
CLINVAR |
Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2.
|
28466842 |
2017 |