Interpret GWAS variant associations across multiple genomics databases
rsID
or
Position
hg38
hg19
Search
Examples:
rs3798220
|
chr6:160540105 (hg38)
|
|
GRCh38
|
GRCh37
Ensembl
Open Targets
Credible Sets
UKB
FinnGen
BBJ
GTEx
eQTL Catalogue
OMIM
GWAS Credible Sets
Open Targets
PheWAS Associations
PheWeb UKB-TOPMed
PheWAS Associations
FinnGen r12
PheWAS Associations
Biobank Japan
GTEx eQTL Associations
GTEx
eQTL Catalogue
EBI eQTL Catalogue
Gene-Disease Associations
Open Targets