DisGeNET - a database of gene-disease associations

KCNJ2, potassium inwardly rectifying channel subfamily J member 2, 3759

N. diseases: 117; N. variants: 33

Disease: ATRIAL FIBRILLATION, FAMILIAL, 9 ×

Variant: rs147750704 ×

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:

rs147750704

rs147750704

Entrez Id:	3759
Gene Symbol:	KCNJ2

KCNJ2

CUI:	C3151431
Disease:

ATRIAL FIBRILLATION, FAMILIAL, 9

A

0.800

CausalMutation

CLINVAR

dbSNP:

rs147750704

rs147750704

Entrez Id:	3759
Gene Symbol:	KCNJ2

KCNJ2

CUI:	C3151431
Disease:

ATRIAL FIBRILLATION, FAMILIAL, 9

0.800

GeneticVariation

UNIPROT