SNP annotation tool query options:
or
| dbSNP ID | Chromosome : |
or
| Batch Query |
Please specify a file: |
SNP annotation tool output:
| Gene SNP Consequences | RefSeq Ensembl Acembly Vega UCSC |
| HapMap population data | CEU YRI CHB JPT |
| Overlaps with | Conserved Transcription Factor Binding Sites (TFBS) |
| Overlaps with | First-Exon and Promoter Prediction (FirstEF) | Overlaps with |
miRBASE 11.0 TargetScan miRNA Regulatory Sites microRNAs (miRNA Registry) / snoRNAs and scaRNAs (snoRNA-LBME-DB) |
| Data from | Genetic Association Studies of Complex Diseases and Disorders (GAD) |
| Structural variations |
Copy Number Polymorphisms from BAC Microarray Analysis (Iafrate) Copy Number Polymorphisms from SNP and BAC microarrays (Redon) Copy Number Polymorphisms from ROMA (Sebat) Copy Number Polymorphisms from BAC Microarray Analysis (Locke) Copy Number Polymorphisms from BAC Microarray Analysis (Sharp) Deletions from Genotype Analysis (Conrad) Deletions from Haploid Hybridization Analysis (Hinds) Deletions from Genotype Analysis (McCarroll) Structural Variation identified by Fosmids (Tuzun) |