rs1054003194
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1057517551
|
|
AT |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1057517763
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1057517764
|
|
AT |
0.700 |
CausalMutation |
CLINVAR |
Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing.
|
24323032 |
2014 |
rs1057517764
|
|
AT |
0.700 |
CausalMutation |
CLINVAR |
Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations.
|
27064304 |
2016 |
rs1060502875
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060502876
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
The contribution of deleterious germline mutations in BRCA1, BRCA2 and the mismatch repair genes to ovarian cancer in the population.
|
24728189 |
2014 |
rs1060502881
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060502882
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060502886
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Prognostic impact of mismatch repair genes germline defects in colorectal cancer patients: are all mutations equal?
|
26485756 |
2015 |
rs1060502888
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Lynch-like syndrome: characterization and comparison with EPCAM deletion carriers.
|
25110875 |
2015 |
rs1060502890
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060502891
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060502903
|
|
GAAGA |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060502918
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060502926
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Germline MSH6 mutations are more prevalent in endometrial cancer patient cohorts than hereditary non polyposis colorectal cancer cohorts.
|
18269114 |
2008 |
rs1060502926
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.
|
24362816 |
2014 |
rs1060502926
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Germline MSH6 mutations are more prevalent in endometrial cancer patient cohorts than hereditary non polyposis colorectal cancer cohorts.
|
18269114 |
2008 |
rs1060502926
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.
|
24362816 |
2014 |
rs1060502926
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Multigene panel analysis identified germline mutations of DNA repair genes in breast and ovarian cancer.
|
26436112 |
2015 |
rs1060502932
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060502937
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060502940
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060502941
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1060502946
|
|
TAA |
0.700 |
CausalMutation |
CLINVAR |
|
|
|