ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from Clinical Genomics Labs, University Health Network and "risk factor" from any submitter

Minimum review status of the submission from Clinical Genomics Labs, University Health Network: Collection method of the submission from Clinical Genomics Labs, University Health Network:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 1
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HGVS dbSNP gnomAD frequency
NM_016222.4(DDX41):c.3G>A (p.Met1Ile) rs141601766 0.00012

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