Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63751319
rs63751319
MSH6 ; FBXO11
A 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
dbSNP: rs63751319
rs63751319
MSH6 ; FBXO11
A 0.700 CausalMutation CLINVAR Molecular and clinical characteristics of MSH6 germline variants detected in colorectal cancer patients. 24100870

2013
dbSNP: rs63751319
rs63751319
MSH6 ; FBXO11
A 0.700 CausalMutation CLINVAR Characterization of two Ashkenazi Jewish founder mutations in MSH6 gene causing Lynch syndrome. 21155762

2011
dbSNP: rs63751319
rs63751319
MSH6 ; FBXO11
A 0.700 CausalMutation CLINVAR Risks of Lynch syndrome cancers for MSH6 mutation carriers. 20028993

2010
dbSNP: rs63751319
rs63751319
MSH6 ; FBXO11
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
dbSNP: rs63751319
rs63751319
MSH6 ; FBXO11
A 0.700 CausalMutation CLINVAR Structure of the human MutSalpha DNA lesion recognition complex. 17531815

2007
dbSNP: rs63751319
rs63751319
MSH6 ; FBXO11
A 0.700 CausalMutation CLINVAR DNA mismatch repair: functions and mechanisms. 16464007

2006
dbSNP: rs63751319
rs63751319
MSH6 ; FBXO11
A 0.700 CausalMutation CLINVAR Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer. 16807412

2006
dbSNP: rs63751319
rs63751319
MSH6 ; FBXO11
A 0.700 CausalMutation CLINVAR DNA mismatch repair. 15952900

2005