An example results file after running finemap_loci.

data("MEX3C")

Format

data.table

SNP

SNP RSID

CHR

Chromosome

POS

Genomic position (in basepairs)

...

Optional: extra columns

Details

Data originally comes from the Parkinson's disease GWAS by Nalls et al. (The Lancet Neurology).

Examples

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)
}