INS, insulin, 3630

N. diseases: 405; N. variants: 37
Disease: Maturity-onset diabetes of the young, type 10 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908260
rs121908260
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10 		0.800 GeneticVariation UNIPROT Structural and functional study of the GlnB22-insulin mutant responsible for maturity-onset diabetes of the young. 25423173 2014
dbSNP: rs121908278
rs121908278
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10 		0.800 GeneticVariation UNIPROT Structural and functional study of the GlnB22-insulin mutant responsible for maturity-onset diabetes of the young. 25423173 2014
dbSNP: rs121908260
rs121908260
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10 		0.800 GeneticVariation UNIPROT Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY). 20226046 2010
dbSNP: rs121908278
rs121908278
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10 		0.800 GeneticVariation UNIPROT Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY). 20226046 2010
dbSNP: rs121908260
rs121908260
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10 		0.800 GeneticVariation UNIPROT Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. 18192540 2008
dbSNP: rs121908260
rs121908260
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10 		0.800 GeneticVariation UNIPROT 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
dbSNP: rs121908278
rs121908278
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10 		0.800 GeneticVariation UNIPROT 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
dbSNP: rs121908278
rs121908278
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10 		0.800 GeneticVariation UNIPROT Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. 18192540 2008
dbSNP: rs121908260
rs121908260
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10 		T 0.800 CausalMutation CLINVAR
dbSNP: rs121908278
rs121908278
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10 		A 0.800 CausalMutation CLINVAR
dbSNP: rs1564911425
rs1564911425
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10 		C 0.700 GeneticVariation CLINVAR INS-gene mutations: from genetics and beta cell biology to clinical disease. 25542748 2015
dbSNP: rs121908259
rs121908259
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10 		0.700 GeneticVariation UNIPROT Structural and functional study of the GlnB22-insulin mutant responsible for maturity-onset diabetes of the young. 25423173 2014
dbSNP: rs121908259
rs121908259
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10 		0.700 GeneticVariation UNIPROT Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY). 20226046 2010
dbSNP: rs1564911425
rs1564911425
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10 		C 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
dbSNP: rs121908259
rs121908259
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10 		0.700 GeneticVariation UNIPROT 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
dbSNP: rs121908259
rs121908259
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10 		0.700 GeneticVariation UNIPROT Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. 18192540 2008
dbSNP: rs1564911425
rs1564911425
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10 		C 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
dbSNP: rs1564911425
rs1564911425
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10 		C 0.700 GeneticVariation CLINVAR Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. 18192540 2008
dbSNP: rs1564911425
rs1564911425
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10 		C 0.700 GeneticVariation CLINVAR Insulin gene mutations as a cause of permanent neonatal diabetes. 17855560 2007
dbSNP: rs886037863
rs886037863
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C3150617
Disease:
Maturity-onset diabetes of the young, type 10 		G 0.700 GeneticVariation CLINVAR