Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs766316400
rs766316400
Entrez Id: 23263
Gene Symbol: MCF2L
MCF2L
CUI: C0030567
Disease:
Parkinson Disease
0.010 GeneticVariation BEFREE Identification of VPS35 p.D620N mutation-related Parkinson's disease in a Taiwanese family with successful bilateral subthalamic nucleus deep brain stimulation: a case report and literature review. 28985717 2017