R/data.R
MEX3C.Rd
An example results file after running finemap_loci.
data("MEX3C")
data.table
SNP RSID
Chromosome
Genomic position (in basepairs)
Optional: extra columns
https://doi.org/10.1016/S1474-4422(19)30320-5
Data originally comes from the Parkinson's disease GWAS by Nalls et al. (The Lancet Neurology).
if (FALSE) { library(echodata) data("Nalls2019_merged") MEX3C <- subset(Nalls2019_merged, Locus=="MEX3C") MEX3C <- echodata::assign_lead_snp(MEX3C) usethis::use_data(MEX3C, overwrite = TRUE) }