Variant: rs12373139 

    present in Gene: MAPT-AS1;SPPL2C
    present in Chromosome: 17
    Position on Chromosome: 45846764
    Alleles of this Variant: G/A

rs12373139 in MAPT-AS1;SPPL2C gene and Corpuscular Hemoglobin Concentration Mean PMID 23222517 2012 Seventy-five genetic loci influencing the human red blood cell.

rs12373139 in MAPT-AS1;SPPL2C gene and Lung Diseases, Interstitial PMID 23583980 2013 Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.

rs12373139 in MAPT-AS1;SPPL2C gene and Parkinson 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.

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

rs12373139 in MAPT-AS1;SPPL2C gene and Primary biliary cirrhosis PMID 22961000 2012 Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.