Variant: rs169201 

    present in Gene: NSF;LRRC37A2
    present in Chromosome: 17
    Position on Chromosome: 46712837
    Alleles of this Variant: A/G

rs169201 in NSF;LRRC37A2 gene and Lung Diseases, Interstitial PMID 23583980 2013 Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.

rs169201 in NSF;LRRC37A2 gene and Parkinson 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 21738487 2011 Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.

rs169201 in NSF;LRRC37A2 gene and ovarian neoplasm PMID 23544013 2013 Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.