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 |
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 |
Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity.
|
28531214 |
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 |
Multigene Panel Testing Provides a New Perspective on Lynch Syndrome.
|
28514183 |
2017 |
rs63750138
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Multigene Panel Testing Provides a New Perspective on Lynch Syndrome.
|
28514183 |
2017 |
rs63750617
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing.
|
27696107 |
2017 |
rs63750854
|
|
GGT |
0.700 |
CausalMutation |
CLINVAR |
Gene panel sequencing in familial breast/ovarian cancer patients identifies multiple novel mutations also in genes others than BRCA1/2.
|
27616075 |
2017 |
rs760190301
|
|
AAGTT |
0.700 |
CausalMutation |
CLINVAR |
Atypical dermal melanocytosis: a diagnostic clue in constitutional mismatch repair deficiency syndrome.
|
28369758 |
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 |
rs1324100572
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Incidental germline variants in 1000 advanced cancers on a prospective somatic genomic profiling protocol.
|
26787237 |
2016 |
rs1553414519
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations.
|
27064304 |
2016 |
rs200492211
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations.
|
27064304 |
2016 |
rs267608059
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Improving performance of multigene panels for genomic analysis of cancer predisposition.
|
26845104 |
2016 |
rs267608076
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Incidental germline variants in 1000 advanced cancers on a prospective somatic genomic profiling protocol.
|
26787237 |
2016 |
rs267608077
|
|
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 |
rs267608077
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Improving performance of multigene panels for genomic analysis of cancer predisposition.
|
26845104 |
2016 |
rs267608092
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
|
27601186 |
2016 |
rs267608094
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
|
27601186 |
2016 |
rs267608118
|
|
CA |
0.700 |
CausalMutation |
CLINVAR |
Prevalence of Pathogenic Mutations in Cancer Predisposition Genes among Pancreatic Cancer Patients.
|
26483394 |
2016 |
rs267608120
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity.
|
26544533 |
2016 |
rs587779212
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
|
27601186 |
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 |
rs587779259
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
|
27601186 |
2016 |