Welcome to ncRNAVar

ncRNAVar is a manually curated database that provides comprehensive experimentally supported associations between noncoding RNA (ncRNA) variants and human disease phenotypes. ncRNAs variants have been experimentally validated as a novel class of biomarkers and potential drug targets for disease diagnosis, therapy and prognosis, and the discovery of relationships between ncRNA variants and disease phenotypes has become increasingly important. ncRNAVar provides experimental validated associations between ncRNA variants and disease phenotypes through manual curation on publications and integration of lncRNA variants from lncRNASNP and GWAS Catalog. ncRNAVar provides user-friendly web interfaces and RESTful application programming interfaces to browse, search, prioritize, analyze and access data freely.

Association data distribution

Contact us

If you have any inquiries, please do not hesitate to contact us via email: liweizhong@mail.sysu.edu.cn or zhangwl25@mail2.sysu.edu.cn