Variant | Chrom | Position | Consequence | Filter | Annotation | ClinVar | Clinical Significance | Allele Frequency | Allele Count | Allele Number | Number of Homozygotes | {{#each variant_list}}
---|---|---|---|---|---|---|---|---|---|---|---|
{{variant_id_label}}{{dbsnp_id}} | {{seq_label}} | {{begin_pos}} | {{hgvs}} | {{filter}} | {{consequence}} | {{#if clinvar_id}} {{clinvar_id}} {{/if}} | {{clinical_significance}} | {{allele_frequency}} | {{allele_count}} | {{allele_num}} | {{num_of_homozygotes}} |