|
rs267608078
|
|
AC |
0.700 |
CausalMutation |
CLINVAR |
Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer.
|
16807412 |
2006 |
|
rs267608078
|
|
AC |
0.700 |
CausalMutation |
CLINVAR |
Molecular and clinical characteristics of MSH6 germline variants detected in colorectal cancer patients.
|
24100870 |
2013 |
|
rs267608078
|
|
AC |
0.700 |
GeneticVariation |
CLINVAR |
Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German Hereditary Nonpolyposis Colorectal Cancer Consortium.
|
15483016 |
2004 |
|
rs267608078
|
|
AC |
0.700 |
GeneticVariation |
CLINVAR |
Feasibility of screening for Lynch syndrome among patients with colorectal cancer.
|
18809606 |
2008 |
|
rs267608078
|
|
AC |
0.700 |
GeneticVariation |
CLINVAR |
Improving performance of multigene panels for genomic analysis of cancer predisposition.
|
26845104 |
2016 |
|
rs267608078
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Risks of Lynch syndrome cancers for MSH6 mutation carriers.
|
20028993 |
2010 |
|
rs267608078
|
|
AC |
0.700 |
CausalMutation |
CLINVAR |
High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry.
|
25117503 |
2014 |
|
rs267608078
|
|
AC |
0.700 |
GeneticVariation |
CLINVAR |
Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.
|
21642682 |
2011 |
|
rs267608078
|
|
AC |
0.700 |
GeneticVariation |
CLINVAR |
Colon and endometrial cancers with mismatch repair deficiency can arise from somatic, rather than germline, mutations.
|
25194673 |
2014 |
|
rs267608078
|
|
AC |
0.700 |
GeneticVariation |
CLINVAR |
Taiwan hospital-based detection of Lynch syndrome distinguishes 2 types of microsatellite instabilities in colorectal cancers.
|
20045164 |
2010 |
|
rs267608078
|
|
AC |
0.700 |
GeneticVariation |
CLINVAR |
Very low prevalence of germline MSH6 mutations in hereditary non-polyposis colorectal cancer suspected patients with colorectal cancer without microsatellite instability.
|
17117178 |
2006 |
|
rs267608078
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Simplified identification of Lynch syndrome: a prospective, multicenter study.
|
22480969 |
2012 |
|
rs267608078
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
High-grade brain tumors in siblings with biallelic MSH6 mutations.
|
21674763 |
2011 |
|
rs267608078
|
|
AC |
0.700 |
GeneticVariation |
CLINVAR |
Risks of Lynch syndrome cancers for MSH6 mutation carriers.
|
20028993 |
2010 |
|
rs267608078
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Novel biallelic mutations in MSH6 and PMS2 genes: gene conversion as a likely cause of PMS2 gene inactivation.
|
17557300 |
2007 |
|
rs267608078
|
|
AC |
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 |
|
rs267608078
|
|
AC |
0.700 |
CausalMutation |
CLINVAR |
Diversity of the clinical presentation of the MMR gene biallelic mutations.
|
24068316 |
2014 |
|
rs267608078
|
|
AC |
0.700 |
GeneticVariation |
CLINVAR |
Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
|
25980754 |
2015 |
|
rs267608078
|
|
AC |
0.700 |
GeneticVariation |
CLINVAR |
High-grade brain tumors in siblings with biallelic MSH6 mutations.
|
21674763 |
2011 |
|
rs267608078
|
|
AC |
0.700 |
CausalMutation |
CLINVAR |
Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.
|
21642682 |
2011 |