rs141322087, ABCC8

N. diseases: 13
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
0.700 GeneticVariation CLINVAR
Short stature
CUI: C0349588
Disease: Short stature
0.700 GeneticVariation CLINVAR
Acid reflux
CUI: C4317146
Disease: Acid reflux
0.700 GeneticVariation CLINVAR
Atrial Septal Defects
CUI: C0018817
Disease: Atrial Septal Defects
0.700 GeneticVariation CLINVAR
Hypoglycemia
CUI: C0020615
Disease: Hypoglycemia
0.700 GeneticVariation CLINVAR
Neonatal respiratory distress
CUI: C4281993
Disease: Neonatal respiratory distress
0.700 GeneticVariation CLINVAR
Neonatal diabetes mellitus
CUI: C0158981
Disease: Neonatal diabetes mellitus
0.700 GeneticVariation CLINVAR
Growth delay
CUI: C0456070
Disease: Growth delay
0.700 GeneticVariation CLINVAR
Macrotia
CUI: C0152421
Disease: Macrotia
0.700 GeneticVariation CLINVAR
Cardiac shunt
CUI: C0232180
Disease: Cardiac shunt
0.700 GeneticVariation CLINVAR
Feeding difficulties
CUI: C0232466
Disease: Feeding difficulties
0.700 GeneticVariation CLINVAR
Small for gestational age (disorder)
CUI: C0235991
Disease: Small for gestational age (disorder)
0.700 GeneticVariation CLINVAR
Large head (disorder)
CUI: C2243051
Disease: Large head (disorder)
0.700 GeneticVariation CLINVAR