ClinVar Miner

Submissions for variant NM_022124.6(CDH23):c.2598C>G (p.Pro866=)

dbSNP: rs2132733015
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002110856 SCV002439682 likely benign not provided 2022-11-01 criteria provided, single submitter clinical testing

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