Overview: rVarBase annotates variants regulatory feature in three fields for lncRNAs, coding genes and microRNAs: chromatin state of the region surrounding variant; regulatory elements overlapped with variant; and variants potential target genes. It also provides optioned extended annotation for variants, including: LD-proxies of known SNP, SNP/CNV that is overlapped with or located in queried variant, traits (disease and expression quantitative trait) associated with variant. rVarBase is an updated version of the database rSNPBase.
Genomic Location: Genomic coordinates through a specific form
Keyword: Search by miRNA name, gene name or lncRNA name, combined with several other features