rs281865071, CHRNB2

N. diseases: 5
Disease: Autosomal Dominant Nocturnal Frontal Lobe Epilepsy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
CUI: C3696898
Disease: Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
0.010 GeneticVariation BEFREE Autosomal dominant nocturnal frontal lobe epilepsy and mild memory impairment associated with CHRNB2 mutation I312M in the neuronal nicotinic acetylcholine receptor. 18534914 2008