MEX3C | R Documentation |
An example results file after running finemap_loci.
data("MEX3C")
data.table
SNP RSID
Chromosome
Genomic position (in basepairs)
Optional: extra columns
Data originally comes from the Parkinson's disease GWAS by Nalls et al. (The Lancet Neurology).
https://doi.org/10.1016/S1474-4422(19)30320-5
## Not run:
library(echodata)
data("Nalls2019_merged")
MEX3C <- subset(Nalls2019_merged, Locus=="MEX3C")
MEX3C <- echodata::assign_lead_snp(MEX3C)
usethis::use_data(MEX3C, overwrite = TRUE)
## End(Not run)
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