NCBI dbSNP Variant Scraper
by parseforge
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. It runs on Apify at $0.0085/result and has 2 users.
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TL;DR: NCBI dbSNP Variant Scraper by parseforge is built for data extraction workflows. It has 2 users and runs on $0.0085/result.
What It Does
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.
Key Stats
- Users
- 2
- Total Runs
- 91
- Pricing
- $0.0085/result
- Rating
- View on Apify →
Quick Answers
Teams that need a ready-made data extraction actor and want to compare pricing, reviews, and actor activity before running it.
Test a small run first, export the sample output, then decide whether the pricing model works for your volume.
parseforge/dbsnp-esummary-scraper
$0.0085/result
Related Docs
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Read guide →Common Questions
What is NCBI dbSNP Variant Scraper?
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.
How much does NCBI dbSNP Variant Scraper cost?
NCBI dbSNP Variant Scraper costs $0.0085/result on Apify, and the free tier lets you test it before upgrading.
Is NCBI dbSNP Variant Scraper free?
NCBI dbSNP Variant Scraper is not fully free, but Apify provides a free tier so you can test it before paying for usage.
How to use NCBI dbSNP Variant Scraper?
Open NCBI dbSNP Variant Scraper on Apify, configure the input for the data you want to scrape, run the actor, and export the results when the run completes.
Free tier available. No credit card needed.
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