DisGeNET - a database of gene-disease associations

rs55884872, 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

CONOTRUNCAL HEART MALFORMATIONS (disorder)

CUI:	C1857586
Disease:	CONOTRUNCAL HEART MALFORMATIONS (disorder)

0.700

GeneticVariation

GWASCAT

Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects.

2017