Variant: rs4837628 

    present in Gene: BRINP1
    present in Chromosome: 9
    Position on Chromosome: 119297431
    Alleles of this Variant: T/C

rs4837628 in BRINP1 gene and Parkinson Disease PMID 20070850 2010 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.