Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1191863771
rs1191863771
APP
CUI: C0037771
Disease: Paraparesis, Spastic
Paraparesis, Spastic 		0.010 GeneticVariation BEFREE A novel presenilin-1 mutation (Leu85Pro) in early-onset Alzheimer disease with spastic paraparesis. 15534188

2004