phenotypes_byid: Get all openSNP known variations and all users sharing that...

In rsnps: Get 'SNP' ('Single-Nucleotide' 'Polymorphism') Data on the Web

Description

Get all openSNP 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 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

Other opensnp-fxns: allgensnp(), allphenotypes(), annotations(), download_users(), fetch_genotypes(), genotypes(), phenotypes(), users()

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
phenotypes_byid(phenotypeid=12, return_ = 'desc', verbose = TRUE)

## End(Not run)

rsnps documentation built on Jan. 28, 2022, 5:07 p.m.