rs281865071, CHRNB2

N. diseases: 5
Disease: Memory impairment ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Memory impairment
CUI: C0233794
Disease: Memory impairment
0.020 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
Memory impairment
CUI: C0233794
Disease: Memory impairment
0.020 GeneticVariation BEFREE The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits. 15964197 2005