rs1191863771, APP

N. diseases: 3
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 novel presenilin-1 mutation (Leu85Pro) in early-onset Alzheimer disease with spastic paraparesis. 15534188 2004