Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs879253853
rs879253853
VPS13C
TTCTG 0.700 CausalMutation CLINVAR Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy. 26942284

2016
dbSNP: rs6812193
rs6812193
FAM47E ; FAM47E-STBD1 ; LOC105377286
T 0.880 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009
dbSNP: rs1564282
rs1564282
GAK
T 0.870 GeneticVariation GWASCAT Genomewide association study for susceptibility genes contributing to familial Parkinson disease. 18985386

2009
dbSNP: rs12817488
rs12817488
CCDC62
T 0.850 GeneticVariation GWASDB Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. 21292315

2011
dbSNP: rs12817488
rs12817488
CCDC62
T 0.850 GeneticVariation GWASCAT Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. 21292315

2011
dbSNP: rs356220
rs356220
SNCA ; LOC105377329
T 0.850 GeneticVariation GWASCAT SNCA_ rs356220 was associated with both Sporadic-PD (OR = 1.37, P = 1 × 10(-9)) and Familial-PD (OR = 1.40, P = 2 × 10(-5)). 24511991

2014
dbSNP: rs356220
rs356220
SNCA ; LOC105377329
T 0.850 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487

2011
dbSNP: rs356220
rs356220
SNCA ; LOC105377329
T 0.850 GeneticVariation GWASCAT Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. 20711177

2010
dbSNP: rs356220
rs356220
SNCA ; LOC105377329
T 0.850 GeneticVariation GWASDB Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. 20711177

2010
dbSNP: rs356220
rs356220
SNCA ; LOC105377329
T 0.850 GeneticVariation GWASCAT Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487

2011
dbSNP: rs356220
rs356220
SNCA ; LOC105377329
T 0.850 GeneticVariation GWASCAT Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. 21084426

2011
dbSNP: rs356220
rs356220
SNCA ; LOC105377329
T 0.850 GeneticVariation GWASDB Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. 21084426

2011
dbSNP: rs356220
rs356220
SNCA ; LOC105377329
T 0.850 GeneticVariation GWASDB SNCA_ rs356220 was associated with both Sporadic-PD (OR = 1.37, P = 1 × 10(-9)) and Familial-PD (OR = 1.40, P = 2 × 10(-5)). 24511991

2014
dbSNP: rs11248051
rs11248051
GAK
T 0.820 GeneticVariation GWASCAT Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. 20711177

2010
dbSNP: rs11248051
rs11248051
GAK
T 0.820 GeneticVariation GWASDB Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. 20711177

2010
dbSNP: rs34372695
rs34372695
RAB25
T 0.810 GeneticVariation GWASDB Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. 21292315

2011
dbSNP: rs34372695
rs34372695
RAB25
T 0.810 GeneticVariation GWASCAT Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. 21292315

2011
dbSNP: rs6599388
rs6599388
TMEM175
T 0.810 GeneticVariation GWASCAT Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. 21292315

2011
dbSNP: rs6599388
rs6599388
TMEM175
T 0.810 GeneticVariation GWASDB Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. 21292315

2011
dbSNP: rs10513789
rs10513789
MCCC1
T 0.800 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487

2011
dbSNP: rs10513789
rs10513789
MCCC1
T 0.800 GeneticVariation GWASCAT Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487

2011
dbSNP: rs11012
rs11012
PLEKHM1
T 0.800 GeneticVariation GWASDB Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. 20070850

2010
dbSNP: rs11012
rs11012
PLEKHM1
T 0.800 GeneticVariation GWASCAT Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. 20070850

2010
dbSNP: rs17115100
rs17115100
CYP17A1 ; WBP1L ; CYP17A1-AS1
T 0.800 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009
dbSNP: rs183211
rs183211
NSF ; LRRC37A2
T 0.800 GeneticVariation GWASCAT Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population. 21812969

2011