appears_in: []
depends_on: []
deprecated: false
description: ClinVar archives reports of relationships among medically important variants
  and phenotypes. It records human variation, interpretations of the relationship
  specific variations to human health, and supporting evidence for each interpretation.
  Each ClinVar record (RCV identifier) represents an aggregated view of interpretations
  of the same variation and condition from one or more submitters (Submitter IDs).
  Submissions for individual variation/phenotype combinations (SCV identifier) are
  also collected and made available separately. This collection references submitters
  (submitter ids) that submit the submissions (SCVs).
example: '26957'
homepage: https://www.ncbi.nlm.nih.gov/clinvar/
keywords: []
mappings:
  miriam: clinvar.submitter
name: ClinVar Submitter
namespace_in_lui: false
pattern: ^\d+$
preferred_prefix: clinvar.submitter
prefix: clinvar.submitter
providers: []
publications: []
synonyms: []
uri_format: https://www.ncbi.nlm.nih.gov/clinvar/submitters/$1
