What sources are used for generating a report?

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
‚ÄčSOURCE
SnpEff
ClinVar
SnpEff
SnpEff
SnpEff
iVariantGuide
dbSNP/1000 genomes
input vcf file
input vcf file
iVariantGuide
iVariantGuide
input vcf file
KEGG
Gene Ontology
2018-08-23T12:22:52+00:00
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