rs142690225, PSEN2

N. diseases: 3
Disease: Dementia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Dementia
CUI: C0497327
Disease: Dementia
0.010 GeneticVariation BEFREE A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairment. 18727676 2008