Variant | Gene | Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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|
|
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 | ||||||
|
|
|
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 | ||||||
|
|
|
C | 0.700 | GeneticVariation | CLINVAR | Insulin gene mutations as a cause of permanent neonatal diabetes. | 17855560 | 2007 | ||||||
|
|
|
C | 0.700 | GeneticVariation | CLINVAR | Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. | 18192540 | 2008 | ||||||
|
|
|
C | 0.700 | GeneticVariation | CLINVAR | INS-gene mutations: from genetics and beta cell biology to clinical disease. | 25542748 | 2015 | ||||||
|
|
|
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 | ||||||
|
|
|
C | 0.700 | GeneticVariation | CLINVAR | Insulin gene mutations as a cause of permanent neonatal diabetes. | 17855560 | 2007 | ||||||
|
|
|
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 | ||||||
|
|
|
C | 0.700 | GeneticVariation | CLINVAR | INS-gene mutations: from genetics and beta cell biology to clinical disease. | 25542748 | 2015 | ||||||
|
|
|
C | 0.700 | GeneticVariation | CLINVAR | Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. | 18192540 | 2008 |