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: a manually curated database for ncRNA variation in human disease

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Welcome to submit your novel association data to the ncRNAVar database:

ncRNAVar encourages users to submit their new association data between ncRNA variants and disease phenotypes for future data integration. The * symbol indicates the required fields.

*ncRNA symbol
*Variation
*Disease phenotype
*Consequence
*PMID
*Validation method(s)
Sample description
Evidential description
Target(s)
Treatment(s)

Bioinformatics Laboratory for Precision Medicine

Copyright @ SUN YAT-SEN UNIVERSITY 2018