Life Sciences

ClinVar (via E-utilities)

The NIH/NLM database of relationships among human genomic variation and phenotype, with supporting evidence. Accessible programmatically via Entrez E-utilities and via a structured FTP feed of XML/JSON variant submissions.

GitHub

Documentation

📖
Documentation
https://www.ncbi.nlm.nih.gov/clinvar/docs/maintenance_use/
📖
Documentation
Linking to ClinVar

API entry from apis.yml

apis.yml Raw ↑ 
name: ClinVar (via E-utilities)
description: The NIH/NLM database of relationships among human genomic variation and phenotype, with supporting
  evidence. Accessible programmatically via Entrez E-utilities and via a structured FTP feed of XML/JSON
  variant submissions.
humanURL: https://www.ncbi.nlm.nih.gov/clinvar/
baseURL: https://eutils.ncbi.nlm.nih.gov/entrez/eutils/
tags:
- Variation
- Clinical Genomics
- NCBI
- ClinVar
properties:
- type: Documentation
  url: https://www.ncbi.nlm.nih.gov/clinvar/docs/maintenance_use/
- type: Documentation
  url: https://www.ncbi.nlm.nih.gov/clinvar/docs/linking/
  title: Linking to ClinVar