clinvar-database

これはレビュー時に保存された抜粋です。完全で最新の内容は外部ソースを確認してください。

---
name: clinvar-database
description: >
  Use when needing clinical significance, pathogenicity classifications (e.g.,
  Pathogenic, Benign, VUS), clinical evidence rationales, or finding "hard
  positive" benchmark controls for human genomic variants.
---

# ClinVar Database

## Prerequisites

1.  **`uv`**: Read the `uv` skill and follow its Setup instructions to ensure
    `uv` is installed and on PATH.
2.  **User Notification**: If .licenses/clinvar_database_LICENSE.txt does not
    already exist in the workspace root directory then (1) prominently notify
    the user to check the terms at https://www.ncbi.nlm.nih.gov/clinvar/, then
    (2) create the file recording the notification text and timestamp.
3.  **`.env` file**: Make sure the `.env` file exists in your home directory.
    Create one if it does not exist.
4.  **`NCBI_API_KEY`** (optional): Raises the NCBI rate limit from 3 to 10
    requests/second. The skill works without it, but a key is recommended if the
    user plans many queries or encounters a 429 error. You can register for a
    key for free at https://www.ncbi.nlm.nih.gov/account/settings/. You **MUST**
    use the safe credentials protocol in the `credentials` skill to check for
    and request this key if this skill looks relevant to the user's request.

## Overview

ClinVar is the primary consensus record for clinical classifications of human
genomic variations. It provides the "clinical ground truth" for pathogenicity
labels (Pathogenic, Likely Pathogenic, Benign, VUS) based on assertions from
global laboratories.

## When to Use

**Use when you need to:**

-   Find the current clinical significance and star rating (review status) for a
    specific variant.
-   Fetch clinician notes, assertion criteria, or rationales for previous
    clinical laboratory classifications.
-   Retrieve the preferred condition name and associated HPO terms for a
    specific variant.
-   Find a list of variant controls (e.g., "Find all Pathogenic variants in the
    HBB gene within 50bp of a signal").
-   Check for conflicting interpretations for a given variant and identify the
    organizations submitting each classification.

**Do NOT use when you need to:**

-   Find specific allele frequencies in global populations (use **gnomAD**).
-   Describe the normal biological role of a protein and typical inheritance
    patterns (use **OMIM**).
-   Predict mechanistic effects of novel mutations, like frameshifts or exon
    skipping (use **AlphaGenome**).
-   Find recommended surveillance schedules for patients with a pathogenic
    variant (use **GeneReviews**).
-   Generate or view 3D structural models of affected proteins (use **PDB /
    AlphaFold**).

## Quick Start

ClinVar queries are executed via a robust Python wrapper script to handle strict
rate limiting and XML/JSON parsing.

Example: Search for BRCA1 variants

```bash
uv run scripts/clinvar_api.py search --query "BRCA1[gene]" --output results.json
```

## Core Rules

-   **Retmax Constraint**: The search command defaults to `--retmax 200`. For
    any "List all" or gene-wide request, you MUST explicitly set `--retmax`
    higher (e.g., 1000) to ensure data completeness.
-   **Use the Wrapper**: Prefer the wrapper script for standard queries. It
    handles rate limiting, retries, and the complex XML parsing for you. If the
    script's parsed output does not contain the specific fields you need, you
    may modify the script or query the NCBI E-utilities API directly — but be
    aware that the raw XML schemas are complex and vary between record types.
-   If the rate limit is hit, the script will throw a clear error. You **MUST**
    use the safe credentials protocol in the `credentials` skill to check for
    and request the `NCBI_API_KEY` to help the user add it to their `.env` file.
-   **Notification**: If this skill is used, ensure this is mentioned in the
    output.

## Utility Scripts

### 1. `count` — Count Matching Variants

**Purpose:** Check ho