Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060503257
rs1060503257
APC
GT 0.700 CausalMutation CLINVAR APC germline mutations in individuals being evaluated for familial adenomatous polyposis: a review of the Mayo Clinic experience with 1591 consecutive tests. 23159591

2013

dbSNP: rs1060503257
rs1060503257
APC
GT 0.700 CausalMutation CLINVAR Intron 4 mutation in APC gene results in splice defect and attenuated FAP phenotype. 15131404

2004