Variant: rs587777482 

    present in Gene: EMP2
    present in Chromosome: 16
    Position on Chromosome: 10547590
    Alleles of this Variant: C/T

rs587777482 in EMP2 gene and NEPHROTIC SYNDROME, TYPE 10 PMID 24814193 2014 Mutations in EMP2 cause childhood-onset nephrotic syndrome.