Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs45539432
rs45539432
PINK1 ; PINK1-AS
0.020 GeneticVariation BEFREE Early-onset Parkinson's disease due to PINK1 p.Q456X mutation--clinical and functional study. 25226871

2014
dbSNP: rs45539432
rs45539432
PINK1 ; PINK1-AS
0.020 GeneticVariation BEFREE The index patient of family W carried a homozygous nonsense mutation (c.1366C>T; p.Q456X) and presented with a phenotype closely resembling idiopathic PD but with an onset at 39 years of age. 16769864

2006