Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63750149
rs63750149
MSH2
CA 0.700 GeneticVariation CLINVAR Reduction in hMSH2 mRNA levels by premature translation termination: implications for mutation screening in hereditary nonpolyposis colorectal cancer. 10080150

1999
dbSNP: rs63750149
rs63750149
MSH2
CA 0.700 CausalMutation CLINVAR