Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387907571
rs387907571
DNAJC13
G 0.800 CausalMutation CLINVAR DNAJC13 mutations in Parkinson disease. 24218364

2014
dbSNP: rs387907571
rs387907571
DNAJC13
0.800 GeneticVariation UNIPROT

dbSNP: rs33939927
rs33939927
LRRK2
A 0.710 CausalMutation CLINVAR The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspot. 27111571

2016
dbSNP: rs33939927
rs33939927
LRRK2
0.710 GeneticVariation BEFREE The Leucine-Rich Repeat Kinase 2 (LRRK2) Gly2019Ser mutation is frequent among Parkinson's disease (PD) patients from the Arab, Jewish, and Iberian populations, while another mutation, Arg1441Gly, is common in the Basque population. 17064949

2007
dbSNP: rs150562946
rs150562946
PRKN
0.700 GeneticVariation UNIPROT Synaptotagmin-11 is a critical mediator of parkin-linked neurotoxicity and Parkinson's disease-like pathology. 29311685

2018
dbSNP: rs34424986
rs34424986
PRKN
0.700 GeneticVariation UNIPROT Synaptotagmin-11 is a critical mediator of parkin-linked neurotoxicity and Parkinson's disease-like pathology. 29311685

2018
dbSNP: rs368134308
rs368134308
PRKN
0.700 GeneticVariation UNIPROT Synaptotagmin-11 is a critical mediator of parkin-linked neurotoxicity and Parkinson's disease-like pathology. 29311685

2018
dbSNP: rs72480422
rs72480422
PRKN
0.700 GeneticVariation UNIPROT Synaptotagmin-11 is a critical mediator of parkin-linked neurotoxicity and Parkinson's disease-like pathology. 29311685

2018
dbSNP: rs764786986
rs764786986
TMEM230
0.700 GeneticVariation UNIPROT Identification of TMEM230 mutations in familial Parkinson's disease. 27270108

2016
dbSNP: rs145242123
rs145242123
DNAJC13
0.700 GeneticVariation UNIPROT DNAJC13 genetic variants in parkinsonism. 25393719

2015
dbSNP: rs146930051
rs146930051
DNAJC13
0.700 GeneticVariation UNIPROT DNAJC13 genetic variants in parkinsonism. 25393719

2015
dbSNP: rs145242123
rs145242123
DNAJC13
0.700 GeneticVariation UNIPROT DNAJC13 mutations in Parkinson disease. 24218364

2014
dbSNP: rs146930051
rs146930051
DNAJC13
0.700 GeneticVariation UNIPROT DNAJC13 mutations in Parkinson disease. 24218364

2014
dbSNP: rs150562946
rs150562946
PRKN
0.700 GeneticVariation UNIPROT PINK1-dependent recruitment of Parkin to mitochondria in mitophagy. 19966284

2010
dbSNP: rs34424986
rs34424986
PRKN
0.700 GeneticVariation UNIPROT PINK1-dependent recruitment of Parkin to mitochondria in mitophagy. 19966284

2010
dbSNP: rs368134308
rs368134308
PRKN
0.700 GeneticVariation UNIPROT PINK1-dependent recruitment of Parkin to mitochondria in mitophagy. 19966284

2010
dbSNP: rs72480422
rs72480422
PRKN
0.700 GeneticVariation UNIPROT PINK1-dependent recruitment of Parkin to mitochondria in mitophagy. 19966284

2010
dbSNP: rs150562946
rs150562946
PRKN
0.700 GeneticVariation UNIPROT Parkin mutations and susceptibility alleles in late-onset Parkinson's disease. 12730996

2003
dbSNP: rs150562946
rs150562946
PRKN
0.700 GeneticVariation UNIPROT Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease. 12629236

2003
dbSNP: rs34424986
rs34424986
PRKN
0.700 GeneticVariation UNIPROT Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease. 12629236

2003
dbSNP: rs34424986
rs34424986
PRKN
0.700 GeneticVariation UNIPROT Parkin mutations and susceptibility alleles in late-onset Parkinson's disease. 12730996

2003
dbSNP: rs368134308
rs368134308
PRKN
0.700 GeneticVariation UNIPROT Parkin mutations and susceptibility alleles in late-onset Parkinson's disease. 12730996

2003
dbSNP: rs368134308
rs368134308
PRKN
0.700 GeneticVariation UNIPROT Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease. 12629236

2003
dbSNP: rs72480422
rs72480422
PRKN
0.700 GeneticVariation UNIPROT Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease. 12629236

2003
dbSNP: rs72480422
rs72480422
PRKN
0.700 GeneticVariation UNIPROT Parkin mutations and susceptibility alleles in late-onset Parkinson's disease. 12730996

2003