DisGeNET - a database of gene-disease associations

Source: GWASDB

Disease: Fibrinogen, CTCAE ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	54798
Gene Symbol:	DCHS2

DCHS2

CUI:	C1561955
Disease:	Fibrinogen, CTCAE

Fibrinogen, CTCAE

0.100

GeneticVariation

GWASDB

Assessment of genetic determinants of the association of γ' fibrinogen in relation to cardiovascular disease.

2011