Variant: rs1078268 

    present in Gene: STH;MAPT
    present in Chromosome: 17
    Position on Chromosome: 45998535
    Alleles of this Variant: A/G

rs1078268 in STH;MAPT gene and Corpuscular Hemoglobin Concentration Mean PMID 23222517 2012 Seventy-five genetic loci influencing the human red blood cell.

rs1078268 in STH;MAPT gene and Parkinson Disease PMID 22438815 2012 Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.

rs1078268 in STH;MAPT gene and Primary biliary cirrhosis PMID 22961000 2012 Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.