rsnps (version 0.0.5)

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.

Value

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

Examples

phenotypes_byid(phenotypeid=12, return_ = 'desc')
phenotypes_byid(phenotypeid=12, return_ = 'knownvars')
phenotypes_byid(phenotypeid=12, return_ = 'users')