Variant: rs393152 

    present in Gene: LINC02210;LINC02210-CRHR1
    present in Chromosome: 17
    Position on Chromosome: 45641777
    Alleles of this Variant: A/G

rs393152 in LINC02210;LINC02210-CRHR1 gene and Corpuscular Hemoglobin Concentration Mean PMID 23222517 2012 Seventy-five genetic loci influencing the human red blood cell.

rs393152 in LINC02210;LINC02210-CRHR1 gene and Corticobasal degeneration PMID 26077951 2015 Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy.

rs393152 in LINC02210;LINC02210-CRHR1 gene and Lung Diseases, Interstitial PMID 23583980 2013 Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.

rs393152 in LINC02210;LINC02210-CRHR1 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 22438815 2012 Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.

PMID 19915575 2009 Genome-wide association study reveals genetic risk underlying Parkinson's disease.

rs393152 in LINC02210;LINC02210-CRHR1 gene and Primary biliary cirrhosis PMID 22961000 2012 Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.

rs393152 in LINC02210;LINC02210-CRHR1 gene and Prion Diseases PMID 22210626 2012 Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.