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Article

Associations between genetic risk variants for kidney diseases and kidney disease etiology.

Scientific reports - 24 Oct 2017

Wunnenburger Sebastian, Schultheiss Ulla T, Walz Gerd, Hausknecht Birgit, Ekici Arif B, Kronenberg Florian, Eckardt Kai-Uwe, Köttgen Anna, Wuttke Matthias

Abstract excerpt

Chronic kidney disease (CKD) is a global health problem with a genetic component. Genome-wide association studies have identified variants associated with specific CKD etiologies, but their genetic overlap has not been well studied. This study examined SNP associations across different CKD etiologies and CKD stages using data from 5,034 CKD patients of the German Chronic Kidney Disease study. In addition to...

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Share to UMOD gene
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polymorphism, Single Nucleotide

Share to Renal Insufficiency, Chronic

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Identifiers

PMID: 29066732
DOI: 10.1038/s41598-017-13356-6
PMCID: PMC5655008

Genes

TNXB
UMOD

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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