The 2.0 version of rSNPBase

Input
Enter your variants (max to 500)
Input of rVarBase could be:
Tips: rVarBase takes hg19 genome coordinates for analysis, other situation please refer to LiftOver for assembly conversion

Option
I. Filter by elements type
TF binding regions     CpG islands    Chromatin interactive regions    
lncRNAs coding regions    Mature miRNAs regions    Target sites of miRNAs   
II. Variant search options
rSNPs rCNVs
        
Input
Enter approved gene symbols (e.g. DRD1)

Option
I. Filter by elements type
TF binding regions     CpG islands    Chromatin interactive regions    
lncRNAs coding regions    Mature miRNAs regions    Target sites of miRNAs   
II. Associated phenotypes help
mRNA abundance Disease
III. Variant search options
rSNPs rCNVs
        
TF name: e.g.STAT3
Gene name: e.g.TOB2
Element option: Variant in predicted binding site
Variant search options: rSNPs rCNVs
               

miRNA name: e.g.hsa-miR-193b-3p
Gene name: e.g.AKT1
Element option: Variant in mature miRNA Variant in predicted target-gene's binding site
Variant search options: rSNPs rCNVs
               

lncRNA name: e.g.lnc-DYRK2-4
Variant search options: rSNPs rCNVs
               

Quick Search:


  
Input of quick search could be:

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Last update: Aug 31, 2015