Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63751693
rs63751693
MSH2
T 0.700 CausalMutation CLINVAR Hereditary non-polyposis colorectal cancer: clinical and molecular evidence for a new entity of hereditary colorectal cancer. 15955785

2005
dbSNP: rs63751693
rs63751693
MSH2
T 0.700 CausalMutation CLINVAR Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer. 15849733

2005
dbSNP: rs63751693
rs63751693
MSH2
T 0.700 CausalMutation CLINVAR Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis. 7726159

1995