Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267608131
rs267608131
MSH6 ; FBXO11
C 0.700 CausalMutation CLINVAR Glioblastomas, astrocytomas and oligodendrogliomas linked to Lynch syndrome. 25648859

2015
dbSNP: rs267608131
rs267608131
MSH6 ; FBXO11
C 0.700 CausalMutation CLINVAR MSH6 mutations are frequent in hereditary nonpolyposis colorectal cancer families with normal pMSH6 expression as detected by immunohistochemistry. 22495361

2012
dbSNP: rs267608131
rs267608131
MSH6 ; FBXO11
C 0.700 CausalMutation CLINVAR Mismatch repair defective breast cancer in the hereditary nonpolyposis colorectal cancer syndrome. 19575290

2010
dbSNP: rs267608131
rs267608131
MSH6 ; FBXO11
C 0.700 CausalMutation CLINVAR Major contribution from recurrent alterations and MSH6 mutations in the Danish Lynch syndrome population. 18566915

2009