Variant: rs12185268 

    present in Gene: MAPT-AS1;SPPL2C
    present in Chromosome: 17
    Position on Chromosome: 45846317
    Alleles of this Variant: A/G

rs12185268 in MAPT-AS1;SPPL2C gene and Corpuscular Hemoglobin Concentration Mean PMID 23222517 2012 Seventy-five genetic loci influencing the human red blood cell.

rs12185268 in MAPT-AS1;SPPL2C gene and Corticobasal degeneration PMID 26077951 2015 Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy.

rs12185268 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 24842889 2014 Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.

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

rs12185268 in MAPT-AS1;SPPL2C gene and Primary biliary cirrhosis PMID 22961000 2012 Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.