rs104894584, KCNJ2

N. diseases: 5
Disease: Ventricular Fibrillation ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Ventricular Fibrillation
CUI: C0042510
Disease: Ventricular Fibrillation
0.010 GeneticVariation BEFREE SQT3 variant (linked to the inward rectifier potassium current I <sub>K1</sub>) of SQTS, results from a gain-of-function mutation (Kir2.1 D172N) in the KCNJ2-encoded channels, which is associated with ventricular fibrillation (VF). 28812984 2017