Welcome to the Bibliome Variant Database

The Bibliome Variant Database is a collection of variants mined from open-access primary literature. All variants included in the database have been mapped to the human genome and are presented in a manner ordered by genomic location. The goal of this database is to provide a searchable structured resource listing variant-containing references.

You are currently using the GRCh38 version of the website.
Click here to use the hg19 version of the website.

Examples - Gene: PCSK9; Variant: 1-55523127-G-T, PCSK9:c.1120G>T, PCSK9:p.D374Y, PCSK9:c.1120G>T; p.D374Y
Genomic Coordinate: Chr1:55523127; Range: Chr1:55523127-55523137

DISCLAIMER: This resource is intended for research purposes only and should not be used during emergencies or as a source of medical or professional advice.