DisGeNET - a database of gene-disease associations

ATRIAL FIBRILLATION, FAMILIAL, 13, C3809311

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	6324
Gene Symbol:	SCN1B

SCN1B

0.700

Biomarker

disease

GENOMICS_ENGLAND

Genetics of Brugada syndrome.

2016

Entrez Id:	6324
Gene Symbol:	SCN1B

SCN1B

0.700

GeneticVariation

disease

UNIPROT

Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation.

2009

Entrez Id:	6324
Gene Symbol:	SCN1B

SCN1B

0.700

Biomarker

disease

GENOMICS_ENGLAND

Short QT syndrome.

2005

Entrez Id:	6324
Gene Symbol:	SCN1B

SCN1B

0.700

Biomarker

disease

CTD_human

Entrez Id:	6324
Gene Symbol:	SCN1B

SCN1B

0.700

GeneticVariation

disease

CLINVAR

Entrez Id:	6324
Gene Symbol:	SCN1B

SCN1B

0.700

CausalMutation

disease

CLINVAR