INS, insulin, 3630

N. diseases: 405; N. variants: 37
Disease: DIABETES MELLITUS, PERMANENT NEONATAL ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80356669
rs80356669
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1833104
Disease:
DIABETES MELLITUS, PERMANENT NEONATAL 		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: rs80356669
rs80356669
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1833104
Disease:
DIABETES MELLITUS, PERMANENT NEONATAL 		0.800 GeneticVariation UNIPROT Insulin gene mutations as a cause of permanent neonatal diabetes. 17855560 2007
dbSNP: rs80356669
rs80356669
Entrez Id: 3630;723961
Gene Symbol: INS;INS-IGF2
INS;INS-IGF2
CUI: C1833104
Disease:
DIABETES MELLITUS, PERMANENT NEONATAL 		A 0.800 CausalMutation CLINVAR