Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3630
Gene Symbol: INS
INS
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.700 GeneticVariation LHGDN Three of the patients with an INS mutation were diagnosed with diabetes between 6 and 12 months of age. 18662362

2008
Entrez Id: 3630
Gene Symbol: INS
INS
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.700 GeneticVariation LHGDN Both the patient and his father (who had childhood-onset insulin-requiring diabetes) were found to be carriers of a heterozygous missense mutation C96Y in exon 3 of the INS gene. 18981553

2008
Entrez Id: 3630
Gene Symbol: INS
INS
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.700 Biomarker LHGDN C-peptide: much more than a byproduct of insulin biosynthesis. 15367890

2004