present in Gene: SNCA
present in Chromosome: 4
Position on Chromosome: 89757390
Alleles of this Variant: G/A;T
rs2736990 in
SNCA gene and
Parkinson Disease
PMID 21738487 2011 Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.
PMID 19915575 2009 Genome-wide association study reveals genetic risk underlying Parkinson's disease.
PMID 22438815 2012 Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
PMID 20070850 2010 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.
PMID 24511991 2014 Identification of a novel Parkinson's disease locus via stratified genome-wide association study.
PMID 20711177 2010 Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.
rs2736990 in
SNCA gene and
Prion Diseases
PMID 22210626 2012 Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.