Here we present a major update of PhenoScanner ('PhenoScanner V2'), including over 150 million genetic variants and more than 65 billion associations (compared to 350 million associations in PhenoScanner V1) with diseases and traits, gene expression, metabolite and protein levels, and epigenetic ...
Kamat MA, et al. PhenoScanner V2: an expanded tool for searching human genotype-phenotype associations. Bioinformatics 2019;35(22):4851-4853. Terms of use Please abide by theterms of useof PhenoScanner when using this R package. About
{r lookup, eval=FALSE} lookup[grepl(",", lookup$rs_id_dbSNP151_GRCh38p7.all_ids),] ``` ## PhenoScanner > PhenoScanner V2 Cardiovascular Epidemiology Unit University of Cambridge Email: phenoscanner@gmail.com > Information: Each user can query a maximum of 500 SNPs, 50 genes or 50 ...
PhenoScanner V2: an expanded tool for searching human genotype–phenotype associations SUMMARY. PhenoScanner is a curated database of publicly available results from large-scale genetic association studies in humans. This online tool facilitates 'phenome scans', where genetic variants are cross-referenced...