rs750414160, KCNJ11

N. diseases: 2
Disease: Congenital Hyperinsulinism ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Congenital Hyperinsulinism
CUI: C3888018
Disease: Congenital Hyperinsulinism
0.010 GeneticVariation BEFREE V290M results in inactivating K(ATP) channels that underlie HI. 20980454 2011