ClinVar Miner

Variants with conflicting interpretations "likely pathogenic" from CIViC knowledgebase, Washington University School of Medicine and "pathogenic" from Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia

Minimum review status of the submission from CIViC knowledgebase, Washington University School of Medicine: Collection method of the submission from CIViC knowledgebase, Washington University School of Medicine:
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_000551.4(VHL):c.208G>A (p.Glu70Lys) rs5030802

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