DisGeNET - a database of gene-disease associations

rs16969925, SCN1B

N. diseases: 6

Disease: Atrial Fibrillation ×

Source: ALL

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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

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Atrial Fibrillation

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.

2009