RIT2, Ras like without CAAX 2, 6014

N. diseases: 46; N. variants: 8
Disease: Adverse effects, not elsewhere classified ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9962013
rs9962013
Entrez Id: 6014
Gene Symbol: RIT2
RIT2
CUI: C0869220
Disease:
Adverse effects, not elsewhere classified 		T 0.700 GeneticVariation GWASCAT Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records. 30420678 2019