Variant: rs199533 

    present in Gene: NSF;LRRC37A2
    present in Chromosome: 17
    Position on Chromosome: 46751565
    Alleles of this Variant: G/A

rs199533 in NSF;LRRC37A2 gene and Corpuscular Hemoglobin Concentration Mean PMID 23222517 2012 Seventy-five genetic loci influencing the human red blood cell.

rs199533 in NSF;LRRC37A2 gene and Lung Diseases, Interstitial PMID 23583980 2013 Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.

rs199533 in NSF;LRRC37A2 gene and Parkinson Disease PMID 19915575 2009 Genome-wide association study reveals genetic risk underlying Parkinson's disease.

PMID 20711177 2010 Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.

PMID 22438815 2012 Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.

PMID 21738487 2011 Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.

rs199533 in NSF;LRRC37A2 gene and Primary biliary cirrhosis PMID 22961000 2012 Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.