Variant: rs1057524896 

    present in Gene: HNRNPUL2-BSCL2;BSCL2
    present in Chromosome: 11
    Position on Chromosome: 62692798
    Alleles of this Variant: C/G

rs1057524896 in HNRNPUL2-BSCL2;BSCL2 gene and Monogenic diabetes PMID 23430896 2012 A Patient with Congenital Generalized Lipodystrophy Due To a Novel Mutation in BSCL2: Indications for Secondary Mitochondrial Dysfunction.