Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267608058
rs267608058
MSH6 ; FBXO11
A 0.700 CausalMutation CLINVAR Frequency of mutations in mismatch repair genes in a population-based study of women with ovarian cancer. 23047549

2012
dbSNP: rs267608058
rs267608058
MSH6 ; FBXO11
A 0.700 CausalMutation CLINVAR Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing. 22006311

2011
dbSNP: rs267608058
rs267608058
MSH6 ; FBXO11
A 0.700 CausalMutation CLINVAR MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer. 20487569

2010
dbSNP: rs267608058
rs267608058
MSH6 ; FBXO11
A 0.700 CausalMutation CLINVAR Major contribution from recurrent alterations and MSH6 mutations in the Danish Lynch syndrome population. 18566915

2009
dbSNP: rs267608058
rs267608058
MSH6 ; FBXO11
A 0.700 CausalMutation CLINVAR Germ-line msh6 mutations in colorectal cancer families. 10537275

1999