Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

GRASP v2.0: an update on the Genome-Wide Repository of Associations between SNPs and phenotypes.

Nucleic acids research - 1 Jan 2015

Eicher John D, Landowski Christa, Stackhouse Brian, Sloan Arielle, Chen Wenjie, Jensen Nicole, Lien Ju-Ping, Leslie Richard, Johnson Andrew D

Abstract excerpt

Here, we present an update on the Genome-Wide Repository of Associations between SNPs and Phenotypes (GRASP) database version 2.0 (http://apps.nhlbi.nih.gov/Grasp/Overview.aspx). GRASP is a centralized repository of publically available genome-wide association study (GWAS) results. GRASP v2.0 contains ∼ 8.87 million SNP associations reported in 2082 studies, an increase of ∼ 2.59 million SNP associations (41.4%...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Databases, Nucleic Acid
Share to Genome-Wide Association Study

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Internet

Share to Phenotype

Share to Polymorphism, Single Nucleotide

Source

Open in PubMed Open full text

Identifiers

PMID: 25428361
DOI: 10.1093/nar/gku1202
PMCID: PMC4383982

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

GRASP v2.0: an update on the Genome-Wide Repository of Associations between SNPs and phenotypes.PMID 25428361Read ↗

GRASP: analysis of genotype-phenotype results from 1390 genome-wide association studies and corresponding open access database.Semantic proximity Read ↗

GWASdb v2: an update database for human genetic variants identified by genome-wide association studies.Semantic proximity Read ↗

The NHGRI-EBI GWAS Catalog, a curated resource of SNP-trait associationsSemantic proximity Read ↗

snpXplorer: a web application to explore human SNP-associations and annotate SNP-sets.Semantic proximity Read ↗

GWASdb: a database for human genetic variants identified by genome-wide association studies.Semantic proximity Read ↗

The NHGRI-EBI GWAS Catalog: knowledgebase and deposition resource.Semantic proximity Read ↗

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations.Semantic proximity Read ↗

webTWAS 2.0: update platform for identifying complex disease susceptibility genes through transcriptome-wide association study.Semantic proximity Read ↗

<i>snpXplorer</i> : a web application to explore SNP-associations and annotate SNP-setsSemantic proximity Read ↗

Exploring genotype-phenotype data using the GWAS CatalogSemantic proximity Read ↗

The EWAS Catalog: a database of epigenome-wide association studiesSemantic proximity Read ↗

The EWAS Catalog: a database of epigenome-wide association studiesSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.