Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1048095
rs1048095
ABCC8
CUI: C1833104
Disease: DIABETES MELLITUS, PERMANENT NEONATAL
DIABETES MELLITUS, PERMANENT NEONATAL 		G 0.810 CausalMutation CLINVAR

dbSNP: rs80356653
rs80356653
ABCC8
CUI: C1833104
Disease: DIABETES MELLITUS, PERMANENT NEONATAL
DIABETES MELLITUS, PERMANENT NEONATAL 		C 0.800 CausalMutation CLINVAR

dbSNP: rs80356651
rs80356651
ABCC8
CUI: C1833104
Disease: DIABETES MELLITUS, PERMANENT NEONATAL
DIABETES MELLITUS, PERMANENT NEONATAL 		T 0.800 CausalMutation CLINVAR

dbSNP: rs80356642
rs80356642
ABCC8
CUI: C1833104
Disease: DIABETES MELLITUS, PERMANENT NEONATAL
DIABETES MELLITUS, PERMANENT NEONATAL 		C 0.800 CausalMutation CLINVAR

dbSNP: rs80356640
rs80356640
ABCC8
CUI: C1833104
Disease: DIABETES MELLITUS, PERMANENT NEONATAL
DIABETES MELLITUS, PERMANENT NEONATAL 		T 0.800 CausalMutation CLINVAR

dbSNP: rs80356637
rs80356637
ABCC8
CUI: C1833104
Disease: DIABETES MELLITUS, PERMANENT NEONATAL
DIABETES MELLITUS, PERMANENT NEONATAL 		G 0.800 CausalMutation CLINVAR

dbSNP: rs80356637
rs80356637
ABCC8
CUI: C1833104
Disease: DIABETES MELLITUS, PERMANENT NEONATAL
DIABETES MELLITUS, PERMANENT NEONATAL 		C 0.800 CausalMutation CLINVAR

dbSNP: rs80356634
rs80356634
ABCC8
CUI: C1833104
Disease: DIABETES MELLITUS, PERMANENT NEONATAL
DIABETES MELLITUS, PERMANENT NEONATAL 		C 0.800 CausalMutation CLINVAR

dbSNP: rs797045213
rs797045213
ABCC8
CUI: C2931832
Disease: Hyperinsulinemic hypoglycemia, familial, 1
Hyperinsulinemic hypoglycemia, familial, 1 		C 0.800 CausalMutation CLINVAR

dbSNP: rs761749884
rs761749884
ABCC8
CUI: C2931832
Disease: Hyperinsulinemic hypoglycemia, familial, 1
Hyperinsulinemic hypoglycemia, familial, 1 		T 0.800 CausalMutation CLINVAR

dbSNP: rs72559734
rs72559734
ABCC8
CUI: C2931832
Disease: Hyperinsulinemic hypoglycemia, familial, 1
Hyperinsulinemic hypoglycemia, familial, 1 		T 0.800 CausalMutation CLINVAR

dbSNP: rs72559723
rs72559723
ABCC8
CUI: C2931832
Disease: Hyperinsulinemic hypoglycemia, familial, 1
Hyperinsulinemic hypoglycemia, familial, 1 		A 0.800 CausalMutation CLINVAR

dbSNP: rs72559715
rs72559715
ABCC8
CUI: C2931832
Disease: Hyperinsulinemic hypoglycemia, familial, 1
Hyperinsulinemic hypoglycemia, familial, 1 		T 0.800 CausalMutation CLINVAR

dbSNP: rs72559713
rs72559713
ABCC8
CUI: C2931832
Disease: Hyperinsulinemic hypoglycemia, familial, 1
Hyperinsulinemic hypoglycemia, familial, 1 		G 0.800 GeneticVariation CLINVAR

dbSNP: rs387906407
rs387906407
ABCC8
CUI: C2931832
Disease: Hyperinsulinemic hypoglycemia, familial, 1
Hyperinsulinemic hypoglycemia, familial, 1 		T 0.800 CausalMutation CLINVAR

dbSNP: rs28936371
rs28936371
ABCC8
CUI: C2931832
Disease: Hyperinsulinemic hypoglycemia, familial, 1
Hyperinsulinemic hypoglycemia, familial, 1 		A 0.800 CausalMutation CLINVAR

dbSNP: rs28936370
rs28936370
ABCC8
CUI: C0271714
Disease: Hypoglycemia, leucine-induced
Hypoglycemia, leucine-induced 		T 0.800 CausalMutation CLINVAR

dbSNP: rs28936370
rs28936370
ABCC8
CUI: C2931832
Disease: Hyperinsulinemic hypoglycemia, familial, 1
Hyperinsulinemic hypoglycemia, familial, 1 		G 0.800 CausalMutation CLINVAR

dbSNP: rs193922400
rs193922400
ABCC8
CUI: C1835887
Disease: DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder)
DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder) 		T 0.800 CausalMutation CLINVAR

dbSNP: rs137852676
rs137852676
ABCC8
CUI: C1833104
Disease: DIABETES MELLITUS, PERMANENT NEONATAL
DIABETES MELLITUS, PERMANENT NEONATAL 		T 0.800 CausalMutation CLINVAR

dbSNP: rs137852674
rs137852674
ABCC8
CUI: C1835887
Disease: DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder)
DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder) 		C 0.800 CausalMutation CLINVAR

dbSNP: rs137852673
rs137852673
ABCC8
CUI: C1835887
Disease: DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder)
DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder) 		A 0.800 CausalMutation CLINVAR

dbSNP: rs137852672
rs137852672
ABCC8
CUI: C2931832
Disease: Hyperinsulinemic hypoglycemia, familial, 1
Hyperinsulinemic hypoglycemia, familial, 1 		T 0.800 CausalMutation CLINVAR

dbSNP: rs137852671
rs137852671
ABCC8
CUI: C2931832
Disease: Hyperinsulinemic hypoglycemia, familial, 1
Hyperinsulinemic hypoglycemia, familial, 1 		T 0.800 CausalMutation CLINVAR

dbSNP: rs193922401
rs193922401
ABCC8
CUI: C0158981
Disease: Neonatal diabetes mellitus
Neonatal diabetes mellitus 		A 0.710 GeneticVariation CLINVAR