Source: CURATED

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908259
rs121908259
INS ; INS-IGF2
CUI: C3150617
Disease: Maturity-onset diabetes of the young, type 10
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
INS ; INS-IGF2
CUI: C3150617
Disease: Maturity-onset diabetes of the young, type 10
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: rs121908259
rs121908259
INS ; INS-IGF2
CUI: C3150617
Disease: Maturity-onset diabetes of the young, type 10
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: rs121908259
rs121908259
INS ; INS-IGF2
CUI: C3150617
Disease: Maturity-onset diabetes of the young, type 10
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