Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs73184656
rs73184656
Entrez Id: 604;100131635
Gene Symbol: BCL6;LOC100131635
BCL6;LOC100131635
CUI: C0869220
Disease:
Adverse effects, not elsewhere classified
C 0.700 GeneticVariation GWASCAT Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records. 30420678 2019