DisGeNET - a database of gene-disease associations

PCIF1, PDX1 C-terminal inhibiting factor 1, 63935

N. diseases: 14; N. variants: 8

Disease: Serum HDL cholesterol measurement ×

The Variant filter does not apply in GDA tabs

Source: ALL

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

Disease

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

CUI:	C0428472
Disease:	Serum HDL cholesterol measurement

Serum HDL cholesterol measurement

0.100

GeneticVariation

phenotype

GWASDB

Common variants at 30 loci contribute to polygenic dyslipidemia.

2009