Variant: rs7224296 

    present in Gene: LRRC37A2;NSF
    present in Chromosome: 17
    Position on Chromosome: 46722680
    Alleles of this Variant: G/A

rs7224296 in LRRC37A2;NSF gene and Corpuscular Hemoglobin Concentration Mean PMID 23222517 2012 Seventy-five genetic loci influencing the human red blood cell.

rs7224296 in LRRC37A2;NSF gene and Intelligence PMID 29326435 2019 A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence.

rs7224296 in LRRC37A2;NSF 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.