rs63750215, PSEN2

N. diseases: 19
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Behavioral Symptoms
CUI: C0004941
Disease: Behavioral Symptoms
0.010 GeneticVariation BEFREE The p.N141I mutation was identified in all affected subjects and was associated with prominent early onset, rapidly progressive dementia, neurologic, and behavioral symptoms. 26166204 2015