Get all openSNP known variations and all users sharing that phenotype for one phenotype(-ID).

phenotypes_byid(
  phenotypeid = NA,
  return_ = c("description", "knownvars", "users"),
  ...
)

Arguments

phenotypeid

ID of openSNP phenotype.

return_

Return data.frame (TRUE) or not (FALSE). Default: FALSE

...

Curl options passed on to crul::HttpClient

Value

List of description of phenotype, list of known variants, or data.frame of variants for each user with that phenotype.

See also

Examples

if (FALSE) { phenotypes_byid(phenotypeid=12, return_ = 'desc') phenotypes_byid(phenotypeid=12, return_ = 'knownvars') phenotypes_byid(phenotypeid=12, return_ = 'users') # pass on curl options phenotypes_byid(phenotypeid=12, return_ = 'desc', verbose = TRUE) }