Variant: rs2078087 

    present in Gene: NMNAT2
    present in Chromosome: 1
    Position on Chromosome: 183389270
    Alleles of this Variant: C/T

rs2078087 in NMNAT2 gene and Alanine aminotransferase measurement PMID 23251661 2012 Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.

rs2078087 in NMNAT2 gene and Aspartate aminotransferase measurement PMID 23251661 2012 Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.

rs2078087 in NMNAT2 gene and Polysomnography PMID 23251661 2012 Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.

rs2078087 in NMNAT2 gene and Serum Alanine Aminotransferase Measurement PMID 23251661 2012 Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.