CHRM2, cholinergic receptor muscarinic 2, 1129

N. diseases: 91; N. variants: 10
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0014544
Disease: Epilepsy
Epilepsy
0.310 GeneticVariation disease BEFREE Genetic polymorphisms of CYP3A5, CHRM2, and ZNF498 and their association with epilepsy susceptibility: a pharmacogenetic and case-control study. 31564953 2019
CUI: C0014544
Disease: Epilepsy
Epilepsy
0.310 Biomarker disease CTD_human Acetylcholine-induced seizure-like activity and modified cholinergic gene expression in chronically epileptic rats. 18333967 2008