rs786201050
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes.
|
28944238 |
2017 |
rs786201084
|
|
AT |
0.700 |
CausalMutation |
CLINVAR |
Multigene Panel Testing Provides a New Perspective on Lynch Syndrome.
|
28514183 |
2017 |
rs864622041
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America.
|
28874130 |
2017 |
rs1057517764
|
|
AT |
0.700 |
CausalMutation |
CLINVAR |
Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations.
|
27064304 |
2016 |
rs1114167767
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Screening for germline mutations in breast/ovarian cancer susceptibility genes in high-risk families in Israel.
|
26687385 |
2016 |
rs146816935
|
|
T |
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 |
rs267608064
|
|
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 |
rs267608076
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Incidental germline variants in 1000 advanced cancers on a prospective somatic genomic profiling protocol.
|
26787237 |
2016 |
rs267608092
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Combined mismatch repair and POLE/POLD1 defects explain unresolved suspected Lynch syndrome cancers.
|
26648449 |
2016 |
rs267608094
|
|
T |
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 |
rs267608118
|
|
CA |
0.700 |
CausalMutation |
CLINVAR |
Prevalence of Pathogenic Mutations in Cancer Predisposition Genes among Pancreatic Cancer Patients.
|
26483394 |
2016 |
rs267608121
|
|
ATCAG |
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 |
rs267608122
|
|
A |
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 |
rs267608122
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
|
27601186 |
2016 |
rs587779212
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Frequent mismatch-repair defects link prostate cancer to Lynch syndrome.
|
27013479 |
2016 |
rs587779227
|
|
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 |
rs587779267
|
|
T |
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 |
rs587779279
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Frequent mismatch-repair defects link prostate cancer to Lynch syndrome.
|
27013479 |
2016 |
rs587779941
|
|
C |
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 |
rs63749942
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Germline multi-gene hereditary cancer panel testing in an unselected endometrial cancer cohort.
|
27443514 |
2016 |
rs63749999
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Inherited Mutations in Women With Ovarian Carcinoma.
|
26720728 |
2016 |
rs63750439
|
|
C |
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 |
rs63750617
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Analysis of Lynch Syndrome Mismatch Repair Genes in Women with Endometrial Cancer.
|
27398995 |
2016 |
rs63750617
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Massively Parallel Sequencing-Based Clonality Analysis of Synchronous Endometrioid Endometrial and Ovarian Carcinomas.
|
26832770 |
2016 |
rs63750617
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
|
27601186 |
2016 |