Variant: rs58926603 

    present in Gene: LOC107985017
    present in Chromosome: 17
    Position on Chromosome: 6438550
    Alleles of this Variant: A/G

rs58926603 in LOC107985017 gene and Hormone measurement PMID 23696881 2013 Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation.

rs58926603 in LOC107985017 gene and Thyroxine measurement PMID 23696881 2013 Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation.