ClinVar Miner

Variants with conflicting interpretations "likely pathogenic" from Claritas Genomics and "pathogenic" from any submitter

Minimum review status of the submission from Claritas Genomics: Collection method of the submission from Claritas Genomics:
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_000124.4(ERCC6):c.1518del (p.Lys506fs) rs786205168

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