Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs72544145
rs72544145
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B
CUI: C3809312
Disease:
ATRIAL FIBRILLATION, FAMILIAL, 14 		0.800 GeneticVariation UNIPROT
dbSNP: rs72544145
rs72544145
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B
CUI: C3809312
Disease:
ATRIAL FIBRILLATION, FAMILIAL, 14 		T 0.800 CausalMutation CLINVAR
dbSNP: rs11607985
rs11607985
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B
CUI: C0202236
Disease:
Triglycerides measurement 		0.700 GeneticVariation GWASDB A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection. 19074352 2008
dbSNP: rs11608072
rs11608072
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B
CUI: C0202236
Disease:
Triglycerides measurement 		0.700 GeneticVariation GWASDB A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection. 19074352 2008
dbSNP: rs17121819
rs17121819
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B
CUI: C3809312
Disease:
ATRIAL FIBRILLATION, FAMILIAL, 14 		0.700 GeneticVariation UNIPROT
dbSNP: rs602594
rs602594
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B
CUI: C0391957
Disease:
idiopathic epilepsy 		0.010 GeneticVariation BEFREE SCN1A rs2298771 was associated in Indians (OR = 0.56, p = 0.005) and SCN2B rs602594 with idiopathic epilepsy (OR = 0.62, p = 0.002). 24337656 2014
dbSNP: rs587777023
rs587777023
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B
CUI: C1142166
Disease:
Brugada Syndrome (disorder) 		0.010 GeneticVariation BEFREE In this work, we identified a novel missense mutation (p.Asp211Gly) in the sodium β2 subunit encoded by SCN2B, in a woman diagnosed with BrS. 23559163 2013
dbSNP: rs1352950843
rs1352950843
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B
CUI: C0004238
Disease:
Atrial Fibrillation 		0.010 GeneticVariation BEFREE We identified 2 nonsynonymous variants in SCN1B (resulting in R85H, D153N) and 2 in SCN2B (R28Q, R28W) in patients with AF. 19808477 2009
dbSNP: rs17121819
rs17121819
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B
CUI: C0004238
Disease:
Atrial Fibrillation 		0.010 GeneticVariation BEFREE We identified 2 nonsynonymous variants in SCN1B (resulting in R85H, D153N) and 2 in SCN2B (R28Q, R28W) in patients with AF. 19808477 2009
dbSNP: rs201460753
rs201460753
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B
CUI: C0004238
Disease:
Atrial Fibrillation 		0.010 GeneticVariation BEFREE We identified 2 nonsynonymous variants in SCN1B (resulting in R85H, D153N) and 2 in SCN2B (R28Q, R28W) in patients with AF. 19808477 2009
dbSNP: rs72544145
rs72544145
Entrez Id: 6327
Gene Symbol: SCN2B
SCN2B
CUI: C0004238
Disease:
Atrial Fibrillation 		0.010 GeneticVariation BEFREE We identified 2 nonsynonymous variants in SCN1B (resulting in R85H, D153N) and 2 in SCN2B (R28Q, R28W) in patients with AF. 19808477 2009