AnyVLM |version| !!!!!!!!!!!!!!!! **AnyVLM** is an off-the-shelf solution for adding local aggregate-level variant information to a `Variant-Level Matching (VLM) network `_. It provides a REST API service that integrates with GA4GH standards for genomic data exchange. AnyVLM enables genomic research organizations to: - **Ingest VCF files** containing variant and allele frequency data - **Register variants** using the GA4GH Variant Representation Specification (VRS) via AnyVar - **Store cohort allele frequencies** (CAF) with zygosity-stratified counts - **Serve VLM protocol-compliant responses** with Beacon handover capabilities This service is designed for rare disease variant frequency tracking in genomic research networks such as `GREGoR `_. If you're setting up AnyVLM for the first time, begin with the :doc:`Getting Started guide `, which covers different installation options. To learn how to use AnyVLM as a service, see :doc:`Usage `. For further assistance, please refer to :doc:`Getting Help `. .. toctree:: :maxdepth: 2 :caption: Contents :hidden: Getting Started Features Usage Configuration API Reference Getting Help Changelog Contributing Project Roadmap License