Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs193922376
rs193922376
MSH2
T 0.700 CausalMutation CLINVAR Screening for Lynch syndrome in colorectal cancer: are we doing enough? 21879275

2012
dbSNP: rs193922376
rs193922376
MSH2
T 0.700 CausalMutation CLINVAR Malignant fibrous histiocytoma is a rare Lynch syndrome-associated tumor in two German families. 21598002

2011
dbSNP: rs193922376
rs193922376
MSH2
T 0.700 CausalMutation CLINVAR The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease. 20682701

2010
dbSNP: rs193922376
rs193922376
MSH2
T 0.700 CausalMutation CLINVAR High risk of endometrial cancer in colorectal cancer kindred is pathognomonic for MMR-mutation carriers. 18841495

2009
dbSNP: rs193922376
rs193922376
MSH2
T 0.700 CausalMutation CLINVAR Mismatch repair gene mutations in Chinese HNPCC patients. 18931482

2008
dbSNP: rs193922376
rs193922376
MSH2
T 0.700 CausalMutation CLINVAR Systematic mRNA analysis for the effect of MLH1 and MSH2 missense and silent mutations on aberrant splicing. 16395668

2006
dbSNP: rs193922376
rs193922376
MSH2
T 0.700 CausalMutation CLINVAR Mutation analysis of MLH1 and MSH2 genes performed by denaturing high-performance liquid chromatography. 11879922

2002
dbSNP: rs193922376
rs193922376
MSH2
T 0.700 CausalMutation CLINVAR Mutation screening of MSH2 and MLH1 mRNA in hereditary non-polyposis colon cancer syndrome. 8880570

1996