Disease: Parkinson Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1994090
rs1994090
Entrez Id: 114134
Gene Symbol: SLC2A13
SLC2A13
CUI: C0030567
Disease:
Parkinson Disease 		0.810 GeneticVariation BEFREE LRRK2 p.Gly2385Arg can explain most if not all of the PD association at rs1994090 in East Asians, but other nonsynonymous variants are independent. 26687033 2016
dbSNP: rs1994090
rs1994090
Entrez Id: 114134
Gene Symbol: SLC2A13
SLC2A13
CUI: C0030567
Disease:
Parkinson Disease 		0.810 GeneticVariation GWASDB Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes. 24842889 2014
dbSNP: rs1994090
rs1994090
Entrez Id: 114134
Gene Symbol: SLC2A13
SLC2A13
CUI: C0030567
Disease:
Parkinson Disease 		0.810 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815 2012
dbSNP: rs1994090
rs1994090
Entrez Id: 114134
Gene Symbol: SLC2A13
SLC2A13
CUI: C0030567
Disease:
Parkinson Disease 		0.810 GeneticVariation GWASCAT Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. 19915576 2009
dbSNP: rs1994090
rs1994090
Entrez Id: 114134
Gene Symbol: SLC2A13
SLC2A13
CUI: C0030567
Disease:
Parkinson Disease 		0.810 GeneticVariation GWASDB Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. 19915576 2009
dbSNP: rs10877840
rs10877840
Entrez Id: 114134
Gene Symbol: SLC2A13
SLC2A13
CUI: C0030567
Disease:
Parkinson Disease 		0.800 GeneticVariation GWASCAT Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. 22451204 2012
dbSNP: rs10877840
rs10877840
Entrez Id: 114134
Gene Symbol: SLC2A13
SLC2A13
CUI: C0030567
Disease:
Parkinson Disease 		0.800 GeneticVariation GWASDB Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. 22451204 2012
dbSNP: rs7304279
rs7304279
Entrez Id: 114134;112268095
Gene Symbol: SLC2A13;LOC112268095
SLC2A13;LOC112268095
CUI: C0030567
Disease:
Parkinson Disease 		0.710 GeneticVariation GWASDB Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes. 24842889 2014
dbSNP: rs7304279
rs7304279
Entrez Id: 114134;112268095
Gene Symbol: SLC2A13;LOC112268095
SLC2A13;LOC112268095
CUI: C0030567
Disease:
Parkinson Disease 		0.710 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815 2012
dbSNP: rs7304279
rs7304279
Entrez Id: 114134;112268095
Gene Symbol: SLC2A13;LOC112268095
SLC2A13;LOC112268095
CUI: C0030567
Disease:
Parkinson Disease 		0.710 GeneticVariation BEFREE The minor alleles at SNPs rs894278, rs1994090, rs2046932, rs4698412, and rs7304279 were found to be significantly higher in cases than in controls, while the minor alleles were found to significantly reduce the risk of developing PD at SNPs rs823128, rs823156, rs6532194, rs1191532, and rs16856139. 21268244 2011
dbSNP: rs1384236
rs1384236
Entrez Id: 114134
Gene Symbol: SLC2A13
SLC2A13
CUI: C0030567
Disease:
Parkinson Disease 		C 0.700 GeneticVariation GWASCAT Genome-wide association study of Parkinson's disease in East Asians. 28011712 2017
dbSNP: rs2708453
rs2708453
Entrez Id: 114134;112268095
Gene Symbol: SLC2A13;LOC112268095
SLC2A13;LOC112268095
CUI: C0030567
Disease:
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes. 24842889 2014
dbSNP: rs4768212
rs4768212
Entrez Id: 114134;112268095
Gene Symbol: SLC2A13;LOC112268095
SLC2A13;LOC112268095
CUI: C0030567
Disease:
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes. 24842889 2014
dbSNP: rs2708453
rs2708453
Entrez Id: 114134;112268095
Gene Symbol: SLC2A13;LOC112268095
SLC2A13;LOC112268095
CUI: C0030567
Disease:
Parkinson Disease 		0.700 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815 2012
dbSNP: rs4768212
rs4768212
Entrez Id: 114134;112268095
Gene Symbol: SLC2A13;LOC112268095
SLC2A13;LOC112268095
CUI: C0030567
Disease:
Parkinson Disease 		0.700 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815 2012