clinvar-database

clinvar-database is a skill for Claude Code, Codex from beita6969/ScienceClaw. It costs 45 tokens per session (3,314 once invoked), scanned A, a copy of clinvar-database, MIT.

A research tool for ClinVar, NCBI's public database of human genetic variants and their reported links to health conditions. It includes classifications such as pathogenic, benign, and uncertain significance.

In plain words
What is it for?
Searching variants by gene, location, condition, or clinical significance; accessing records through NCBI's APIs or bulk files; and adding ClinVar classifications to VCF files, which store genetic variant calls.
Why use it?
It helps locate clinical evidence and compare interpretations of genetic variants from different reports. It also shows review status and can identify disagreements between classifications.

Skill for Claude CodeCodex

Written for no agent in particular: nothing here depends on one. Also seen: positional $N argument.

Good fit Searching variants by gene, location, condition, or clinical significance; accessing records through NCBI's APIs or bulk files; and adding ClinVar classifications to VCF files, which store genetic variant calls.

Compare 6 skills from other repositories ↓
Install with agentmods
npx agentmods add skills/beita6969/scienceclaw/clinvar-database
Install

Getting it into your agent

One page per mod, every tool's command on it. A separate URL per tool would split the same page into five that compete with each other.

Any agent
npx skills add beita6969/ScienceClaw --skill clinvar-database
Clone the repo
git clone --depth 1 https://github.com/beita6969/ScienceClaw

Made for: Claude Code, Codex.

Wrote this? Show the measurements

A badge with what this costs and how it scanned, read live from this page, so it follows the numbers instead of freezing them. Markdown for a README, HTML for a documentation site or a project page.

agentmods badge for clinvar-database

README.md
[![agentmods](https://agentmods.dev/badge/skills/beita6969/scienceclaw/clinvar-database.svg)](https://agentmods.dev/skills/beita6969/scienceclaw/clinvar-database)
Your own site
<a href="https://agentmods.dev/skills/beita6969/scienceclaw/clinvar-database"><img src="https://agentmods.dev/badge/skills/beita6969/scienceclaw/clinvar-database.svg" alt="Measured on agentmods" height="20"></a>
Per session 45 Skills are progressive disclosure: only the name and description are preloaded; the body loads when the skill is used.
When invoked 3,314 The whole file, excluding the scripts and references it only reads on demand.
Security scan A 1 finding. A grade says what 26 rules found in the file — not that it is safe.
Origin 88% copy Near-identical to another mod in the catalogue.
Token cost

What it costs to keep this loaded

Counted locally with the o200k_base tokenizer, which is exact for GPT models; Claude uses its own tokenizer and its counts differ. Treat this as one consistent yardstick across the catalogue rather than a bill. Prices are per million input tokens.

ModelPer sessionOnce invoked
Fable 5.1 $0.00045 $0.03314
Opus 5 $0.00023 $0.01657
Sonnet 5 $0.00009 $0.00663
Haiku 4.5 $0.00005 $0.00331

Measured 9d ago against content hash 976110f1deb5, method: parsed. Prices are Anthropic first-party input rates as of 2026-09-08, from the pricing page.

Security

Grade A, and why

clinvar-database scanned grade A with 1 finding against 26 rules in 11 categories — prompt injection, anti-refusal, data exfiltration, privilege escalation, supply chain, agent snooping, system-prompt leakage, SSRF and excessive agency — measured 9d ago.

A static scan of the body, not an audit. Every finding is printed with the line that produced it so you can judge whether it matters here. A mod is markdown that instructs an agent; that is exactly why what it instructs is worth reading.

Makes network callslowCapability

Not a fault in itself. Listed so you know the mod talks to something, and to what.

**Quick example using curl:**
Origin

This is a copy

88% identical to clinvar-database — 6 lines differ, which has more behind it and is treated as the original. This page carries a canonical link to it rather than competing with it.

skills/clinvar-database/SKILL.md · 362 lines

How it starts

The opening of the file, as written. The whole thing — 362 lines — stays where its author put it; the contents beside it link to each section on GitHub.

ClinVar Database

Overview

ClinVar is NCBI's freely accessible archive of reports on relationships between human genetic variants and phenotypes, with supporting evidence. The database aggregates information about genomic variation and its relationship to human health, providing standardized variant classifications used in clinical genetics and research.

When to Use This Skill

This skill should be used when:

  • Searching for variants by gene, condition, or clinical significance
  • Interpreting clinical significance classifications (pathogenic, benign, VUS)
  • Accessing ClinVar data programmatically via E-utilities API
  • Downloading and processing bulk data from FTP
  • Understanding review status and star ratings
  • Resolving conflicting variant interpretations
  • Annotating variant call sets with clinical significance

Core Capabilities

1. Search and Query ClinVar

Web Interface Queries

Search ClinVar using the web interface at https://www.ncbi.nlm.nih.gov/clinvar/

Common search patterns:

  • By gene: BRCA1[gene]
  • By clinical significance: pathogenic[CLNSIG]
  • By condition: breast cancer[disorder]
  • By variant: NM_000059.3:c.1310_1313del[variant name]
  • By chromosome: 13[chr]
  • Combined: BRCA1[gene] AND pathogenic[CLNSIG]
Programmatic Access via E-utilities

Access ClinVar programmatically using NCBI's E-utilities API. Refer to references/api_reference.md for comprehensive API documentation including:

  • esearch - Search for variants matching criteria
  • esummary - Retrieve variant summaries
  • efetch - Download full XML records
  • elink - Find related records in other NCBI databases

Quick example using curl:

# Search for pathogenic BRCA1 variants
curl "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esearch.fcgi?db=clinvar&term=BRCA1[gene]+AND+pathogenic[CLNSIG]&retmode=json"

Best practices:

  • Test queries on the web interface before automating
  • Use API keys to increase rate limits from 3 to 10 requests/second
  • Implement exponential backoff for rate limit errors
  • Set Entrez.email when using Biopython

Read the full file on GitHub · 362 lines

Changes

What this file has done since we first saw it

Hashed on every crawl. A supply-chain change to an agent config is a question of when, not whether, so the history is kept rather than the latest state alone.

  1. 9d ago First seen · 362 lines · 45 tokens per session scan A 976110f1deb5

Subscribe to this mod's changes

clinvar-database is a skill published in the GitHub repository beita6969/ScienceClaw (896 stars, last pushed 3mo ago), licensed MIT. It adds 45 tokens to every session and 3,314 once invoked, about $0.0002 per session on Opus 5. A static security scan graded it A with 1 finding (makes network calls). It is 88% identical to clinvar-database, differing in 6 lines, and is treated as a copy.

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