Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs34424986
rs34424986
PRKN
CUI: C4275179
Disease: Young onset Parkinson disease
Young onset Parkinson disease 		0.710 GeneticVariation BEFREE The compound heterozygous mutation c.951G>C (p.G284R) and c.924C>T (p.R275W) is the pathogenic factor in this EOPD Uyghur family. 24831986

2014