Disease: Parkinson Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2068143
rs2068143
Entrez Id: 83464
Gene Symbol: APH1B
APH1B
CUI: C0030567
Disease:
Parkinson Disease 		0.010 GeneticVariation BEFREE Significant correlation with CSF Aβ42 levels in PD was observed for two SNPs, (APP rs466448 and APH1B rs2068143). 25808939 2015