Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3630
Gene Symbol: INS
INS
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia 		0.700 GeneticVariation CLINVAR INS-gene mutations: from genetics and beta cell biology to clinical disease. 25542748

2015
Entrez Id: 3630
Gene Symbol: INS
INS
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia 		0.700 GeneticVariation CLINVAR Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY). 20226046

2010
Entrez Id: 3630
Gene Symbol: INS
INS
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia 		0.700 GeneticVariation CLINVAR Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. 18192540

2008
Entrez Id: 3630
Gene Symbol: INS
INS
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia 		0.700 GeneticVariation CLINVAR 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. 18162506

2008
Entrez Id: 3630
Gene Symbol: INS
INS
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia 		0.700 GeneticVariation CLINVAR Insulin gene mutations as a cause of permanent neonatal diabetes. 17855560

2007
Entrez Id: 3630
Gene Symbol: INS
INS
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia 		0.700 Biomarker HPO