Variant: rs121908259 

    present in Gene: INS;INS-IGF2
    present in Chromosome: 11
    Position on Chromosome: 2160955
    Alleles of this Variant: C/T

rs121908259 in INS;INS-IGF2 gene and Maturity-onset diabetes of the young, type 10 PMID 25423173 2014 Structural and functional study of the GlnB22-insulin mutant responsible for maturity-onset diabetes of the young.

PMID 20226046 2010 Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY).

PMID 18192540 2008 Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes.

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.