CAUSALdb

Genome-Wide Association Studies Catalog

The Genome-Wide Association Studies (GWAS) Catalog provides a consistent, searchable, visualisable and freely available database of published SNP-trait associations, which can be easily integrated wit ...

GWAS Atlas

The GWAS Atlas is a manually curated resource of genome-wide variant-trait associations for a wide range of species.

WheatQTLdb

WheatQTLdb is a manually curated QTL database for wheat that includes information about QTL identified through interval mapping and MTA identified using GWAS.

GWASdb

GWASdb comprises of collections of traits/diseases associated SNP (TASs) from current GWAS and their comprehensive functional annotations, as well as disease classifications.

Biobank Japan PheWeb

This website releases genome-wide association study (GWAS) summary statistics of the BioBank Japan Project (BBJ). We provide GWAS results in the Japanese population (mainly from BBJ) using the PheWeb ...

webTWAS

The webTWAS integrates large number of GWAS summary level data for disease, and this number will be constantly increasing according to our timely curation. The webTWAS calculates the causal genes usin ...

Idiopathic Pulmonary Fibrosis (IPF) Genome-wide Association Study

Meta-analysis of GWAS of IPF susceptibility. Building up on published GWAS results (PMID: 24429156, 23583980, 29066090) and novel study samples to identify novel genes and further advance in the under ...

Ontology for Genetic Disease Investigations

This ontology is used to model scientific investigation, especially Genome-Wide Association Studies (GWAS), to discover genetic susceptibility factors to disease, such as Diabetes. It models the genet ...

GWAS Diagram Browser

ALSGENE

The publicly available database, which houses findings from genetic-association studies in amyotrophic lateral sclerosis, showcases meta-analyses of GWAS data and allows researchers to compare their o ...

GWASkb

We have built an information extraction system called GWASkb that parses the biomedical literature to automatically extract associations between traits and genomic variants that have been discovered v ...

DistiLD Database: Diseases and Traits in Linkage Disequilibrium Blocks

The DistiLD database aims to increase the usage of existing genome-wide association studies (GWAS) results by making it easy to query and visualize disease-associated SNPs and genes in their chromosom ...

Database of Genotypes and Phenotypes

The Database of Genotypes and Phenotypes (dbGaP) archives and distributes the results of studies that have investigated the interaction of genotype and phenotype. Such studies include genome-wide asso ...

dbInDel

A database of enhancer-associated insertion and deletion variants by analysis of H3K27ac ChIP-Seq. Cancer hallmarks rely on its specific transcriptional programs, which are dysregulated by multiple m ...

PheWAS

Phenome-wide association studies (PheWAS) analyze many phenotypes compared to a single genetic variant (or other attribute). This method was originally described using electronic medical record (EMR) ...

DISEASES

DISEASES is a weekly updated web resource that integrates evidence on disease-gene associations from automatic text mining, manually curated literature, cancer mutation data, and genome-wide associati ...

Human Ancestry Ontology

The Human Ancestry Ontology (HANCESTRO) provides a systematic description of the ancestry concepts used in the NHGRI-EBI Catalog of published genome-wide association studies.

circVAR database

circVAR database is genome-wide archive of genetic variants for human circular RNAs Circular RNAs (circRNAs), the 3' and 5' ends of which are covalently linked, are a kind of widely distributed and ab ...

EWAS Catalog

A database of epigenome-wide association studies.