Search by ClinVar Variants (in JoGo)

e.g. ALDH2_chr12_111761933_111822532, HBB_chr11_5220464_5232071.

e.g. ALDH2, BRCA1.

Chromosome name (e.g., chr11).

ClinVar clinical significance classification.

Impact severity level (e.g., HIGH, MODERATE, LOW, MODIFIER).

Detailed annotation impact classification.

Start genomic position (GRCh38).

End genomic position (GRCh38).

Exact genomic position (GRCh38).

Choose a field to sort by.

Ascending / Descending.

Results per page.

Please provide at least one search criterion: genename, regionname, pos, snpeff annotation impact, or clinsig.