Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63750767
rs63750767
MSH6 ; FBXO11
TTCAAAAGGGACATAGAAAA 0.700 CausalMutation CLINVAR A cohort analysis of men with a family history of BRCA1/2 and Lynch mutations for prostate cancer. 27456091

2016
dbSNP: rs63750767
rs63750767
MSH6 ; FBXO11
TTCAAAAGGGACATAGAAAA 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
dbSNP: rs63750767
rs63750767
MSH6 ; FBXO11
TTCAAAAGGGACATAGAAAA 0.700 CausalMutation CLINVAR Improving performance of multigene panels for genomic analysis of cancer predisposition. 26845104

2016
dbSNP: rs63750767
rs63750767
MSH6 ; FBXO11
TTCAAAAGGGACATAGAAAA 0.700 CausalMutation CLINVAR Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel. 25186627

2015
dbSNP: rs63750767
rs63750767
MSH6 ; FBXO11
TTCAAAAGGGACATAGAAAA 0.700 CausalMutation CLINVAR Combined Microsatellite Instability, MLH1 Methylation Analysis, and Immunohistochemistry for Lynch Syndrome Screening in Endometrial Cancers From GOG210: An NRG Oncology and Gynecologic Oncology Group Study. 26552419

2015
dbSNP: rs63750767
rs63750767
MSH6 ; FBXO11
TTCAAAAGGGACATAGAAAA 0.700 CausalMutation CLINVAR Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome. 25980754

2015
dbSNP: rs63750767
rs63750767
MSH6 ; FBXO11
TTCAAAAGGGACATAGAAAA 0.700 CausalMutation CLINVAR Molecular and clinical characteristics of MSH6 germline variants detected in colorectal cancer patients. 24100870

2013
dbSNP: rs63750767
rs63750767
MSH6 ; FBXO11
TTCAAAAGGGACATAGAAAA 0.700 CausalMutation CLINVAR Characterization of two Ashkenazi Jewish founder mutations in MSH6 gene causing Lynch syndrome. 21155762

2011
dbSNP: rs63750767
rs63750767
MSH6 ; FBXO11
TTCAAAAGGGACATAGAAAA 0.700 CausalMutation CLINVAR High frequency of exon deletions and putative founder effects in French Canadian Lynch syndrome families. 19459153

2009
dbSNP: rs63750767
rs63750767
MSH6 ; FBXO11
TTCAAAAGGGACATAGAAAA 0.700 CausalMutation CLINVAR Feasibility of screening for Lynch syndrome among patients with colorectal cancer. 18809606

2008
dbSNP: rs63750767
rs63750767
MSH6 ; FBXO11
TTCAAAAGGGACATAGAAAA 0.700 CausalMutation CLINVAR Structure of the human MutSalpha DNA lesion recognition complex. 17531815

2007
dbSNP: rs63750767
rs63750767
MSH6 ; FBXO11
TTCAAAAGGGACATAGAAAA 0.700 CausalMutation CLINVAR DNA mismatch repair: functions and mechanisms. 16464007

2006
dbSNP: rs63750767
rs63750767
MSH6 ; FBXO11
TTCAAAAGGGACATAGAAAA 0.700 CausalMutation CLINVAR DNA mismatch repair. 15952900

2005