Pricing

from $7.50 / 1,000 results

NCBI dbSNP Variant Scraper

Search NCBI dbSNP for short genetic variants by gene symbol or rs ID. Returns rs accession, chromosome position, allele info, gene context, and global minor allele frequencies. Useful for GWAS pipelines, variant annotation, population genetics, and pharmacogenomics work.

Pricing

from $7.50 / 1,000 results

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0.0

(0)

Developer

ParseForge

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Monthly active users

2 days ago

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Automation

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Developer tools

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, you’ll need an Apify account and your API token, found in Integrations settings in Apify Console.

Python

JavaScript

CLI

OpenAPI

HTTP

MCP

1import { ApifyClient } from 'apify-client';
2
3// Initialize the ApifyClient with your Apify API token
4// Replace the '<YOUR_API_TOKEN>' with your token
5const client = new ApifyClient({
6    token: '<YOUR_API_TOKEN>',
7});
8
9// Prepare Actor input
10const input = {
11    "maxItems": 10,
12    "searchTerm": "BRCA1"
13};
14
15// Run the Actor and wait for it to finish
16const run = await client.actor("parseforge/dbsnp-esummary-scraper").call(input);
17
18// Fetch and print Actor results from the run's dataset (if any)
19console.log('Results from dataset');
20console.log(`💾 Check your data here: https://console.apify.com/storage/datasets/${run.defaultDatasetId}`);
21const { items } = await client.dataset(run.defaultDatasetId).listItems();
22items.forEach((item) => {
23    console.dir(item);
24});
25
26// 📚 Want to learn more 📖? Go to → https://docs.apify.com/api/client/js/docs

NCBI dbSNP Variant Scraper API in JavaScript

The Apify API client for JavaScript is the official library that allows you to use NCBI dbSNP Variant Scraper API in JavaScript or TypeScript, providing convenience functions and automatic retries on errors.

Install the apify-client

$npm install apify-client

Other API clients include:

NCBI dbSNP Variant Scraper API in Python

NCBI dbSNP Variant Scraper API through CLI

NCBI dbSNP Variant Scraper OpenAPI definition

NCBI dbSNP Variant Scraper API

NCBI dbSNP Variants Scraper

parseforge/ncbi-dbsnp-variants-scraper

Discover medical and biomedical records from Ncbi Dbsnp Variants with names, identifiers, classifications, descriptions, status and source links. Ideal for healthcare research, pharma teams and clinical analytics. Run on demand or on a recurring schedule and feed every row into your favourite ana.

ParseForge

HPO Human Phenotype Ontology Scraper

parseforge/hpo-phenotypes-scraper

Search the Human Phenotype Ontology by keyword or HP ID and pull back terms with hpoId, name, definition, synonyms, parents, children, plus optional associated diseases and genes. Useful for rare disease research, clinical curation, and genomic variant annotation pipelines.

ParseForge

Ensembl Genomics Scraper (Genes, Variants, Sequences)

parseforge/ensembl-genomics-scraper

Query the Ensembl genome reference for 200+ species. Look up genes by symbol or stable ID, list features in a genomic region, fetch DNA sequence, or resolve human variants (rsIDs). Returns biotype, coordinates, transcript IDs, descriptions, and assembly metadata.

ParseForge

NCBI ClinVar Variants Scraper - Genetic Variation Data

parseforge/ncbi-clinvar-variants-scraper

Sweep medical and biomedical records from Ncbi Clinvar Variants with names, identifiers, classifications, descriptions, status and source links. Ideal for healthcare research, pharma teams and clinical analytics. Run on demand or on a recurring schedule and feed every row into your favourite anal.

ParseForge

NCBI ClinVar Variant Scraper

parseforge/clinvar-esummary-scraper

Query NCBI ClinVar for human genetic variants tied to disease. Search by gene symbol, variant ID, or clinical significance and pull variation IDs, gene info, molecular consequence, clinical assertions, and review status. Useful for clinical genomics, variant curation, and research.

ParseForge

Clinical Trial Multi-Source Aggregator

parseforge/clinical-trial-multi-source-scraper

Search active and historical clinical trials across the EU CTIS, WHO, openFDA and ClinVar variants in one query. Pull trial IDs, sponsors, phases, conditions, locations, status and outcome data. Built for pharma research, patient navigators and biotech analysts.

ParseForge

Instagram Reels Scraper

scraper-engine/instagram-reels-scraper

Instagram Reels Scraper lets you extract reels data quickly and efficiently. Gather video URLs, captions, hashtags, likes, views, comments, and user profiles. Ideal for research, analytics, and trend tracking with fast, reliable, and easy automation.

Scraper Engine

186

4.7

(12)

PubMed Scraper

labrat011/pubmed-scraper

Search 35M+ medical citations from PubMed/MEDLINE. Extract articles, abstracts, authors, MeSH terms, and citations for research, competitive intelligence, or AI/RAG pipelines. No API key required.

mick_

PubMed Scraper for RAG: Papers as Chunked JSON

devanshlive/pubmed-rag-extractor

Scrape PubMed citations by search term, MeSH, and article type. Returns RAG-ready JSON with full-text chunks from PMC Open Access (cl100k_base, 512/50) and abstract fallback. Drop-in for LangChain, LlamaIndex, Qdrant, Pinecone, Weaviate, pgvector. Skip GROBID / Pubmed Parser. $0.02 per paper.

Devansh Tiwari

HGNC Gene Symbols Scraper

parseforge/hgnc-gene-symbols-scraper

Query the HUGO Gene Nomenclature Committee database for approved human gene symbols, names, aliases, chromosomal location, gene family, RefSeq, Ensembl, OMIM, UniProt, and external links. Export to JSON, CSV, or Excel for bioinformatics, genomics research, and pharmaceutical pipelines.

ParseForge