Disease: Atrial Fibrillation, Familial, 4 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs74315449
rs74315449
Entrez Id: 9992;105372791
Gene Symbol: KCNE2;LOC105372791
KCNE2;LOC105372791
CUI: C1862394
Disease:
Atrial Fibrillation, Familial, 4 		0.800 GeneticVariation UNIPROT Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation. 15368194 2004
dbSNP: rs74315449
rs74315449
Entrez Id: 9992;105372791
Gene Symbol: KCNE2;LOC105372791
KCNE2;LOC105372791
CUI: C1862394
Disease:
Atrial Fibrillation, Familial, 4 		T 0.800 GeneticVariation CLINVAR Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation. 15368194 2004
dbSNP: rs74315449
rs74315449
Entrez Id: 9992;105372791
Gene Symbol: KCNE2;LOC105372791
KCNE2;LOC105372791
CUI: C1862394
Disease:
Atrial Fibrillation, Familial, 4 		T 0.800 CausalMutation CLINVAR