Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1011490341
rs1011490341
Entrez Id: 3751
Gene Symbol: KCND2
KCND2
CUI: C0235480
Disease:
Paroxysmal atrial fibrillation 		0.010 GeneticVariation BEFREE Through genetic studies, we showed that autosomal dominant early-onset nocturnal paroxysmal AF is caused by p.S447R mutation in KCND2, encoding the pore-forming (α) subunit of the Kv4.2 cardiac potassium channel. 30571183 2018