Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs774847203
rs774847203
APC
T 0.700 GeneticVariation CLINVAR Germline APC mutation spectrum derived from 863 genomic variations identified through a 15-year medical genetics service to French patients with FAP. 20685668

2010
dbSNP: rs774847203
rs774847203
APC
T 0.700 GeneticVariation CLINVAR Analysis of the human APC mutation spectrum in a saccharomyces cerevisiae strain with a mismatch repair defect. 12494469

2003