ClinVar Miner

Variants with conflicting interpretations "likely benign" from Clinical Genomics Labs, University Health Network and "benign" 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: 2
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HGVS dbSNP gnomAD frequency
NM_000551.4(VHL):c.74C>T (p.Pro25Leu) rs35460768 0.00261
NM_000551.4(VHL):c.150C>G (p.Ala50=) rs61751580 0.00070

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