Variant: rs10445337 

    present in Gene: MAPT
    present in Chromosome: 17
    Position on Chromosome: 45990034
    Alleles of this Variant: T/C

rs10445337 in MAPT gene and Corpuscular Hemoglobin Concentration Mean PMID 23222517 2012 Seventy-five genetic loci influencing the human red blood cell.

rs10445337 in MAPT gene and Parkinson Disease PMID 22438815 2012 Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.

rs10445337 in MAPT gene and Primary biliary cirrhosis PMID 22961000 2012 Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.