Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4157
Gene Symbol: MC1R
MC1R 		0.020 GeneticVariation disease BEFREE MC1R variants in Chinese Han patients with sporadic Parkinson's disease. 27084066 2016
Entrez Id: 6531
Gene Symbol: SLC6A3
SLC6A3 		0.040 GeneticVariation disease BEFREE SLC6A3 rs28363170 and rs3836790 variants in Han Chinese patients with sporadic Parkinson's disease. 27353511 2016
Entrez Id: 6622
Gene Symbol: SNCA
SNCA 		0.100 GeneticVariation disease BEFREE SNCA rs356182 variant increases risk of sporadic Parkinson's disease in ethnic Chinese. 27538639 2016
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2 		0.100 Biomarker disease BEFREE Leucine-rich repeat kinase 2 (LRRK2) has been linked to familial and sporadic Parkinson's disease. 28041945 2017
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2 		0.100 Biomarker disease BEFREE Leucine-rich repeat kinase 2 gene (LRRK2) was recognized associated with both familial and sporadic Parkinson Disease (PD). 28131193 2017
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2 		0.100 Biomarker disease BEFREE Leucine-rich repeat kinase 2 (LRRK2) is a recently discovered molecule associated with familial and sporadic Parkinson's disease. 28168579 2017
Entrez Id: 7421
Gene Symbol: VDR
VDR 		0.010 GeneticVariation disease BEFREE Vitamin D receptor gene polymorphisms, smoking, and risk of sporadic Parkinson's disease in Japan. 28216333 2017
Entrez Id: 6622
Gene Symbol: SNCA
SNCA 		0.100 Biomarker disease BEFREE Alpha-synuclein (α-syn) is involved in both familial and sporadic Parkinson's disease (PD). 28790323 2017
Entrez Id: 7124
Gene Symbol: TNF
TNF 		0.030 GeneticVariation disease BEFREE TNF-α -308 G/A and -238 G/A promoter polymorphisms and sporadic Parkinson's disease in an Italian cohort. 29406912 2018
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2 		0.100 GeneticVariation disease BEFREE LRRK2 p.G2385R is an Asian specific genetic risk factor for sporadic Parkinson's disease. 29414410 2018
Entrez Id: 6622
Gene Symbol: SNCA
SNCA 		0.100 Biomarker disease BEFREE α-synuclein is involved in both familial and sporadic Parkinson's disease. 29702063 2018
Entrez Id: 65018
Gene Symbol: PINK1
PINK1 		0.070 Biomarker disease BEFREE PTEN induced putative kinase 1 (PINK1), also known as PARK6, is causally linked to familial Parkinsonism, and heterozygous loss of PINK1 is a risk factor for sporadic Parkinson's disease. 29843233 2018
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2 		0.100 GeneticVariation disease BEFREE LRRK2 links genetic and sporadic Parkinson's disease. 30837320 2019
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2 		0.100 Biomarker disease BEFREE Leucine-rich repeat kinase 2 (LRRK2) is a molecule associated with familial and sporadic Parkinson's disease. 31555076 2019
Entrez Id: 7054
Gene Symbol: TH
TH 		0.010 GeneticVariation disease BEFREE Tyrosine hydroxylase polymorphism in familial and sporadic Parkinson's disease. 7913740 1994
Entrez Id: 6622
Gene Symbol: SNCA
SNCA 		0.100 Biomarker disease BEFREE Alpha synuclein is present in Lewy bodies in sporadic Parkinson's disease. 9857974 1998
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2 		0.100 GeneticVariation disease BEFREE G2019S LRRK2 mutation in familial and sporadic Parkinson's disease in Russia. 17044089 2006
Entrez Id: 4521
Gene Symbol: NUDT1
NUDT1 		0.020 GeneticVariation disease BEFREE A valine to methionine polymorphism at codon 83 in the 8-oxo-dGTPase gene MTH1 is not associated with sporadic Parkinson's disease. 11136354 2000
Entrez Id: 120892
Gene Symbol: LRRK2
LRRK2 		0.100 GeneticVariation disease BEFREE A common leucine-rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in Russia. 17388990 2007
Entrez Id: 6622
Gene Symbol: SNCA
SNCA 		0.100 GeneticVariation disease BEFREE A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson disease. 30146727 2018
Entrez Id: 130013
Gene Symbol: ACMSD
ACMSD 		0.010 GeneticVariation disease BEFREE A Novel p.Glu298Lys Mutation in the ACMSD Gene in Sporadic Parkinson's Disease. 28671144 2017
Entrez Id: 9474
Gene Symbol: ATG5
ATG5 		0.010 PosttranslationalModification disease BEFREE A novel and functional variant within the ATG5 gene promoter in sporadic Parkinson's disease. 23384565 2013
Entrez Id: 7345
Gene Symbol: UCHL1
UCHL1 		0.090 GeneticVariation disease BEFREE A polymorphic variation of serine to tyrosine at codon 18 in the ubiquitin C-terminal hydrolase-L1 gene is associated with a reduced risk of sporadic Parkinson's disease in a Japanese population. 11535241 2001
Entrez Id: 7345
Gene Symbol: UCHL1
UCHL1 		0.090 GeneticVariation disease BEFREE A protective effect of a UCH-L1 variant, S18Y, was suggested since the common variant was found to be inversely associated with sporadic Parkinson's disease (PD). 17287139 2007
Entrez Id: 9627
Gene Symbol: SNCAIP
SNCAIP 		0.020 GeneticVariation disease BEFREE A putative polymorphic Val44Ala variation in the synphilin-1 gene is undetectable in Japanese sporadic Parkinson's disease patients. 11784370 2002