rs63750577, PSEN1

N. diseases: 8
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
0.010 GeneticVariation BEFREE The clinical phenotype was consistent regarding initial memory impairment and early onset in the late twenties found in all S170F patients. 29466804 2018