DisGeNET - a database of gene-disease associations

High density lipoprotein measurement, C0392885

Variant: rs17231506 ×

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

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs17231506

CETP

0.800

GeneticVariation

GWASCAT

Genetic architecture of human plasma lipidome and its link to cardiovascular disease.

31551469

2019

dbSNP:

rs17231506

CETP

0.800

GeneticVariation

GWASCAT

Genetic analyses of diverse populations improves discovery for complex traits.

31217584

2019

dbSNP:

rs17231506

CETP

0.800

GeneticVariation

GWASCAT

A large electronic-health-record-based genome-wide study of serum lipids.

29507422

2018

dbSNP:

rs17231506

CETP

0.800

GeneticVariation

GWASCAT

The impact of low-frequency and rare variants on lipid levels.

25961943

2015

dbSNP:

rs17231506

CETP

0.800

GeneticVariation

GWASDB

Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.

23063622

2012

dbSNP:

rs17231506

CETP

0.800

GeneticVariation

GWASDB

Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project.

22629316

2012