rs1994090, SLC2A13

N. diseases: 2
Disease: Parkinson Disease ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Parkinson Disease
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
Parkinson Disease
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
Parkinson Disease
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
Parkinson Disease
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
Parkinson Disease
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