Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1135
Gene Symbol: CHRNA2
CHRNA2 		0.700 GeneticVariation disease UNIPROT Mutation of CHRNA2 in a family with benign familial infantile seizures: Potential role of nicotinic acetylcholine receptor in various phenotypes of epilepsy. 25847220 2015
Entrez Id: 1135
Gene Symbol: CHRNA2
CHRNA2 		0.700 Biomarker disease GENOMICS_ENGLAND Increased sensitivity of the neuronal nicotinic receptor alpha 2 subunit causes familial epilepsy with nocturnal wandering and ictal fear. 16826524 2006
Entrez Id: 1135
Gene Symbol: CHRNA2
CHRNA2 		0.700 GeneticVariation disease UNIPROT Increased sensitivity of the neuronal nicotinic receptor alpha 2 subunit causes familial epilepsy with nocturnal wandering and ictal fear. 16826524 2006
Entrez Id: 1135
Gene Symbol: CHRNA2
CHRNA2 		0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 1135
Gene Symbol: CHRNA2
CHRNA2 		0.700 Biomarker disease CTD_human
Entrez Id: 1135
Gene Symbol: CHRNA2
CHRNA2 		0.700 CausalMutation disease CLINVAR
Entrez Id: 1137
Gene Symbol: CHRNA4
CHRNA4 		0.100 CausalMutation disease CLINVAR
Entrez Id: 1141
Gene Symbol: CHRNB2
CHRNB2 		0.100 CausalMutation disease CLINVAR