rs759680369
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Diversity of genetic events associated with MLH1 promoter methylation in Lynch syndrome families with heritable constitutional epimutation.
|
29790873 |
2018 |
rs1060500699
|
|
GT |
0.700 |
CausalMutation |
CLINVAR |
Spectrum of mismatch repair gene mutations and clinical presentation of Hispanic individuals with Lynch syndrome.
|
28449805 |
2017 |
rs1060500699
|
|
GT |
0.700 |
CausalMutation |
CLINVAR |
A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America.
|
28874130 |
2017 |
rs267607871
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.
|
27978560 |
2017 |
rs267607871
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer.
|
28135145 |
2017 |
rs863225378
|
|
ATCTGGACC |
0.700 |
CausalMutation |
CLINVAR |
Multigene Panel Testing Provides a New Perspective on Lynch Syndrome.
|
28514183 |
2017 |
rs1057517541
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
|
27601186 |
2016 |
rs267607717
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
|
27601186 |
2016 |
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 |
rs267607723
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations.
|
27064304 |
2016 |
rs267607759
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
|
27601186 |
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 |
rs267607867
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
|
27601186 |
2016 |
rs267607901
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
[Founder mutation in Lynch syndrome].
|
27295708 |
2016 |
rs267607903
|
|
TAAAC |
0.700 |
CausalMutation |
CLINVAR |
[Founder mutation in Lynch syndrome].
|
27295708 |
2016 |
rs267607906
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
[Founder mutation in Lynch syndrome].
|
27295708 |
2016 |
rs41542214
|
|
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 |
rs587778888
|
|
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 |
rs63750948
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome.
|
27435373 |
2016 |
rs63751153
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations.
|
27064304 |
2016 |
rs63751662
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
|
27601186 |
2016 |
rs730881734
|
|
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 |
rs878853787
|
|
TA |
0.700 |
CausalMutation |
CLINVAR |
[Founder mutation in Lynch syndrome].
|
27295708 |
2016 |
rs1060500699
|
|
GT |
0.700 |
CausalMutation |
CLINVAR |
Selective Versus Universal Screening for Lynch Syndrome: A Six-Year Clinical Experience.
|
24903654 |
2015 |
rs1434898623
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mutation spectrum and risk of colorectal cancer in African American families with Lynch syndrome.
|
26248088 |
2015 |