rs63750524, PSEN1

N. diseases: 2
Disease: Paraparesis, Spastic ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Paraparesis, Spastic
CUI: C0037771
Disease: Paraparesis, Spastic
0.010 GeneticVariation BEFREE A presenilin 1 mutation (Arg278Ser) associated with early onset Alzheimer's disease and spastic paraparesis. 17507029 2007