Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587779075
rs587779075
MSH2
T 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
dbSNP: rs587779075
rs587779075
MSH2
T 0.700 CausalMutation CLINVAR Patients with Lynch syndrome mismatch repair gene mutations are at higher risk for not only upper tract urothelial cancer but also bladder cancer. 22883484

2013
dbSNP: rs587779075
rs587779075
MSH2
T 0.700 CausalMutation CLINVAR Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome. 21642682

2011
dbSNP: rs587779075
rs587779075
MSH2
T 0.700 CausalMutation CLINVAR High frequency of exon deletions and putative founder effects in French Canadian Lynch syndrome families. 19459153

2009
dbSNP: rs587779075
rs587779075
MSH2
T 0.700 CausalMutation CLINVAR A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome. 15235030

2004
dbSNP: rs587779075
rs587779075
MSH2
T 0.700 CausalMutation CLINVAR Mismatch repair gene defects contribute to the genetic basis of double primary cancers of the colorectum and endometrium. 10196371

1999