Variant: rs1057524907 

    present in Gene: INS-IGF2;INS
    present in Chromosome: 11
    Position on Chromosome: 2159907
    Alleles of this Variant: T/C

rs1057524907 in INS-IGF2;INS gene and Hyperglycemia PMID 25542748 2015 INS-gene mutations: from genetics and beta cell biology to clinical disease.

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.

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

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

rs1057524907 in INS-IGF2;INS gene and Monogenic diabetes 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 17855560 2007 Insulin gene mutations as a cause of permanent neonatal diabetes.

PMID 25542748 2015 INS-gene mutations: from genetics and beta cell biology to clinical disease.

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.