rsnps (version 0.2.0)

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

Description

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

Usage

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 GET.

Value

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

Examples

# NOT RUN {
phenotypes_byid(phenotypeid=12, return_ = 'desc')
phenotypes_byid(phenotypeid=12, return_ = 'knownvars')
phenotypes_byid(phenotypeid=12, return_ = 'users')

# pass on curl options
library("httr")
phenotypes_byid(phenotypeid=12, return_ = 'desc', 
  config=c(verbose(), timeout(1)))
phenotypes_byid(phenotypeid=12, return_ = 'desc', config=verbose())
# }