DisGeNET - a database of gene-disease associations

rs1448817, None

N. diseases: 1

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

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Atrial Fibrillation

CUI:	C0004238
Disease:	Atrial Fibrillation

0.700

GeneticVariation

GWASDB

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.

2009

Atrial Fibrillation

CUI:	C0004238
Disease:	Atrial Fibrillation

0.700

GeneticVariation

GWASDB

Variants conferring risk of atrial fibrillation on chromosome 4q25.

2007