Variant: rs121908272 

    present in Gene: INS;INS-IGF2
    present in Chromosome: 11
    Position on Chromosome: 2160887
    Alleles of this Variant: G/C

rs121908272 in INS;INS-IGF2 gene and DIABETES MELLITUS, PERMANENT NEONATAL PMID 18162506 2008 Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.

PMID 17855560 2007 Insulin gene mutations as a cause of permanent neonatal diabetes.