Finds all variants in a VCF, 23andMe, or AncestryDNA file that have matching entries in the ClinVar database.
Height prediction demo for WGS (Whole Genome Sequencing) .vcf files
Uses the GENCODE gene annotations on the human reference genome. Can also display variant call files (VCF (WGS), 23andMe, AncestryDNA). Check the screenshots below to get a glimpse of the main features.