Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs141322087
rs141322087
ABCC8
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs141322087
rs141322087
ABCC8
CUI: C4281993
Disease: Neonatal respiratory distress
Neonatal respiratory distress 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs141322087
rs141322087
ABCC8
CUI: C0349588
Disease: Short stature
Short stature 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs141322087
rs141322087
ABCC8
CUI: C0235991
Disease: Small for gestational age (disorder)
Small for gestational age (disorder) 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs141322087
rs141322087
ABCC8
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs141322087
rs141322087
ABCC8
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs141322087
rs141322087
ABCC8
CUI: C0456070
Disease: Growth delay
Growth delay 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs141322087
rs141322087
ABCC8
CUI: C0152421
Disease: Macrotia
Macrotia 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs141322087
rs141322087
ABCC8
CUI: C0232180
Disease: Cardiac shunt
Cardiac shunt 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs141322087
rs141322087
ABCC8
CUI: C0020615
Disease: Hypoglycemia
Hypoglycemia 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs141322087
rs141322087
ABCC8
CUI: C4317146
Disease: Acid reflux
Acid reflux 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs141322087
rs141322087
ABCC8
CUI: C0158981
Disease: Neonatal diabetes mellitus
Neonatal diabetes mellitus 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs141322087
rs141322087
ABCC8
CUI: C2243051
Disease: Large head (disorder)
Large head (disorder) 		T 0.700 GeneticVariation CLINVAR