ClinVar Miner

Submissions for variant NM_022124.6(CDH23):c.2059+18G>A

gnomAD frequency: 0.00003  dbSNP: rs201712138
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002039955 SCV002108672 likely benign not provided 2024-05-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002039955 SCV005228191 likely benign not provided criteria provided, single submitter not provided

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