DisGeNET - a database of gene-disease associations

KCNJ11, potassium inwardly rectifying channel subfamily J member 11, 3767

N. diseases: 218; N. variants: 80

Disease: DIABETES MELLITUS, PERMANENT NEONATAL ×

Variant: rs115716690 ×

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:

rs115716690

rs115716690

Entrez Id:	3767
Gene Symbol:	KCNJ11

KCNJ11

CUI:	C1833104
Disease:

DIABETES MELLITUS, PERMANENT NEONATAL

0.700

GeneticVariation

UNIPROT