Related Servers

No user-submitted related servers found.

Related Servers

• Folklore Clinical Variant

  helena-bioinformatics

  A

  license

  -Not graded

  quality

  B

  maintenance

  Bioinformatics MCP for genomic variant interpretation, gene-disease evidence and literature. Folklore 1.5.0 adds read-only ClinGen gene-to-disease and disease-to-gene lookups alongside GRCh38 germline variant interpretation and biomedical literature. Seven tools; public information only; qualified professional review required.

  Updated 2 days ago (2026-09-11 13:08 UTC)

  Apache 2.0

• clingen-link

  berntpopp

  A

  license

  -Not graded

  quality

  A

  maintenance

  Enables querying ClinGen curated evidence for gene-disease validity, dosage, actionability, and variant pathogenicity via MCP tools.

  Updated 2 days ago (2026-09-11 22:46 UTC)

  MIT
• 

  OpenCRAVATofficial

  KarchinLab

  F

  license

  -Not graded

  quality

  C

  maintenance

  Annotate variants by with a deep and rich set of data. Can annotate: genetic change, rsID, CAid, HGVS (g./c./p.), protein change.

  Updated 2 months ago (2026-07-15 17:26 UTC)

  5

  -

• gnomAD MCP Server

  koido

  A

  license

  B

  quality

  D

  maintenance

  Provides a programmatic interface to the Genome Aggregation Database (gnomAD) API across versions v2.1.1, v3.1.2, and v4.1.0. It enables users to query gene metadata, variant information, population frequencies, and ClinVar data through a unified schema.

  Updated 8 months ago (2026-01-23 08:10 UTC)

  12

  6

  Apache 2.0

• @cyanheads/gnomad-genetics-mcp

  cyanheads

  A

  license

  -Not graded

  quality

  A

  maintenance

  Look up variant allele frequencies by ancestry, gene loss-of-function constraint, gene variant lists, and sequencing coverage over gnomAD — with ClinVar significance joined in — via MCP.

  Updated 13 days ago (2026-08-31 02:40 UTC)

  44 npm

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  Apache 2.0

• EVEE MCP Server

  goodfire-ai

  F

  license

  A

  quality

  F

  maintenance

  Provides interpretable variant effect predictions for 4.2 million ClinVar variants using the EVEE API. Enables searching, comparing, and analyzing genetic variants with AI-generated mechanistic interpretations and disruption profiles.

  Updated 4 months ago (2026-05-20 21:30 UTC)

  6

  17

  -