DisGeNET - a database of gene-disease associations

SCN2B, sodium voltage-gated channel beta subunit 2, 6327

N. diseases: 33; N. variants: 8

Disease: Atrial Fibrillation ×

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

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

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

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

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