Variant: rs415430 

    present in Gene: WNT3;LRRC37A2
    present in Chromosome: 17
    Position on Chromosome: 46781778
    Alleles of this Variant: C/T

rs415430 in WNT3;LRRC37A2 gene and Corpuscular Hemoglobin Concentration Mean PMID 23222517 2012 Seventy-five genetic loci influencing the human red blood cell.

rs415430 in WNT3;LRRC37A2 gene and Lung Diseases, Interstitial PMID 23583980 2013 Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.

rs415430 in WNT3;LRRC37A2 gene and Parkinson Disease PMID 21812969 2011 Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.

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