We provide annotations from dbSNP, ClinVar, and 1000 Genomes in addition to all sources contained in our KnowledgeBase, iBioGuide. We also provide links to additional information in iBioGuide as well as external sites such as OMIM, MedGen, and more. At this time iVariantGuide does not support user-defined annotation sources. If there is a specific database you would like us to support, please let us know!
| FILTER Variant Class Clinical Significance Functional Class Impact Region Zygosity Allele Frequency Depth Distribution Quality Length of Indel Substitution Types Chromosomal Location Pathways GO Terms |
SOURCE SnpEff ClinVar SnpEff SnpEff SnpEff iVariantGuide dbSNP/1000 genomes input vcf file input vcf file iVariantGuide iVariantGuide input vcf file KEGG Gene Ontology |