rs281865071, CHRNB2

N. diseases: 5
Disease: Forgetful ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Forgetful
CUI: C0542476
Disease: Forgetful
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