rs63751399, PSEN1

N. diseases: 3
Disease: Presenile dementia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
0.010 GeneticVariation BEFREE Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation. 11094121 2000