Disease: Parkinson Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs864309527
rs864309527
Entrez Id: 116442
Gene Symbol: RAB39B
RAB39B
CUI: C0030567
Disease:
Parkinson Disease 		0.010 GeneticVariation BEFREE The RAB39B p.G192R mutation causes X-linked dominant Parkinson's disease. 26399558 2015