Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80356667
rs80356667
INS ; INS-IGF2
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: rs80356667
rs80356667
INS ; INS-IGF2
0.800 GeneticVariation UNIPROT Insulin gene mutations as a cause of permanent neonatal diabetes. 17855560

2007
dbSNP: rs80356667
rs80356667
INS ; INS-IGF2
A 0.800 CausalMutation CLINVAR