Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267607767
rs267607767
MLH1
G 0.700 CausalMutation CLINVAR A multifactorial likelihood model for MMR gene variant classification incorporating probabilities based on sequence bioinformatics and tumor characteristics: a report from the Colon Cancer Family Registry. 22949379

2013
dbSNP: rs267607767
rs267607767
MLH1
G 0.700 CausalMutation CLINVAR An American founder mutation in MLH1. 21671475

2012
dbSNP: rs267607767
rs267607767
MLH1
G 0.700 CausalMutation CLINVAR Classifying MLH1 and MSH2 variants using bioinformatic prediction, splicing assays, segregation, and tumor characteristics. 19267393

2009
dbSNP: rs267607767
rs267607767
MLH1
G 0.700 CausalMutation CLINVAR Interpretation of genetic test results for hereditary nonpolyposis colorectal cancer: implications for clinical predisposition testing. 10422993

1999
dbSNP: rs267607767
rs267607767
MLH1
G 0.700 CausalMutation CLINVAR In vitro transcription/translation assay for the screening of hMLH1 and hMSH2 mutations in familial colon cancer. 7557107

1995