NCBI dbSNP Variant Scraper
Pricing
from $7.50 / 1,000 results
Scrapes variant summary records from NCBI dbSNP for a given search term and returns each variant as a flat row with clinical significance, allele frequencies, gene mappings, and PubMed IDs.
Pricing
from $7.50 / 1,000 results
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ParseForge
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15 days ago
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You can access the NCBI dbSNP Variant Scraper programmatically from your own applications by using the Apify API. You can also choose the language preference from below. To use the Apify API, youโll need an Apify account and your API token, found in API & Integrations in Apify Console.
{ "mcpServers": { "apify": { "type": "http", "url": "https://mcp.apify.com/?tools=fetch-actor-details,parseforge/dbsnp-esummary-scraper" } }}The configuration above connects to the hosted Apify MCP server with the dbSNP Scraper - NCBI Variant Summary Data Extraction Actor already loaded. It uses OAuth, so your client opens a browser window to sign you in to Apify on first use. No API token is needed. Clients without OAuth support can authenticate with an Authorization: Bearer header carrying an API token from API & Integrations in Apify Console.
Get a ready-to-use configuration for your MCP client with the dbSNP Scraper - NCBI Variant Summary Data Extraction Actor preconfigured at https://mcp.apify.com/?tools=fetch-actor-details,parseforge/dbsnp-esummary-scraper.
You can connect to the Apify MCP Server using clients like Tester MCP Client, or any other MCP client of your choice.
If you want to learn more about our Apify MCP implementation, check out our MCP documentation. To learn more about the Model Context Protocol in general, refer to the official MCP documentation or read our blog post.