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myvariant

pipeworx.ioInfrastructure

No liveness check has reached it yet; it has been in the index since 10 Oct 2026. How this is checked

Myvariant is an HTTP JSON-RPC MCP server exposing tools to search and retrieve aggregated human genetic-variant annotations. It combines sources such as dbSNP, ClinVar, CADD, dbNSFP, and gnomAD for researchers and bioinformatics applications.

Inferred · not functionally tested

WebAPICloud-managed
myvariant preview
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Overview

6 features

Purpose: Finding and interpreting aggregated annotations for human genetic variants across multiple biomedical databases.

Inferred · not functionally tested

Audience: geneticists, biomedical researchers, and bioinformatics developers

Inferred · not functionally tested

Functions: data_extraction

Inferred · not functionally tested

Interfaces: API: indicated (inferred, not tested) · MCP: indicated (inferred, not tested) · CLI: unknown · Self-hosting: unknown

Recorded constraints: pricing: unknown · license: Proprietary · platforms: WEB · deployment: browser, api_only, cloud_managed

Constraint provenance is unknown; confirm requirements with the publisher.

Record sources: gateway.pipeworx.io. These links do not verify the individual claims.

myvariant is an API design, testing & docs project. Inferred · not functionally tested: It focuses on finding and interpreting aggregated annotations for human genetic variants across multiple biomedical databases. Inferred · not functionally tested: It is built as a B2B product for geneticists, biomedical researchers, and bioinformatics developers. Basis unknown · not verified: It ships for the web and API.

Pipeworx builds and maintains myvariant. Inferred · not functionally tested: Key capabilities include variant search, HGVS lookup, and clinVar annotations. Inferred · not functionally tested: Catalogued interfaces include an MCP server and a public API.

Summary written by a language model from the project’s public pages.

Tasks: Inferred · not functionally tested

  • Variant search
  • HGVS lookup
  • ClinVar annotations
  • gnomAD frequencies
  • CADD scores
  • dbNSFP scores

Topics: Inferred · not functionally tested

Tags
genetic-variantsvariant-annotationmcp-serverbioinformatics

JSON profile · Text profile · Access guide

Built with & integrations

Hosting
Cloudflare
Connectors
MCPAPI
Runs on
BrowserAPI-onlyCloud-managed
Detected from
Cloudflare
cf-ray header

Trust & compliance

Public signals
HTTPS

Indexing history

1

What PulseGate has recorded for this listing

  1. Indexed10 Oct · 00:02 UTC
    Myvariant seen via MCP Registry (official)
    Source: MCP Registry (official) · Open

Frequently asked questions about myvariant

What does myvariant do?
Inferred · not functionally tested: Myvariant focuses on finding and interpreting aggregated annotations for human genetic variants across multiple biomedical databases. It is catalogued under API design, testing & docs on PulseGate.
Who is myvariant for?
Inferred · not functionally tested: myvariant is a B2B product built for geneticists, biomedical researchers, and bioinformatics developers.
What platforms does myvariant run on?
Basis unknown · not verified: myvariant runs on the web and API.
Is myvariant still maintained?
Unverified. myvariant has not been re-checked since it entered the index, so there is no finding either way — and only a positive finding would say otherwise.
Who develops myvariant?
myvariant is developed by Pipeworx.
Does myvariant have an API or integrations?
Inferred · not functionally tested: Yes — myvariant exposes an MCP server and a public API.

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