ClinVar Miner

Variants with conflicting interpretations "pathogenic" from Centre for Mendelian Genomics, University Medical Centre Ljubljana and "likely benign" from any submitter

Minimum review status of the submission from Centre for Mendelian Genomics, University Medical Centre Ljubljana: Collection method of the submission from Centre for Mendelian Genomics, University Medical Centre Ljubljana:
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_004004.6(GJB2):c.71G>A (p.Trp24Ter) rs104894396 0.00002

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