ClinVar Miner

Submissions for variant NM_022124.6(CDH23):c.2289+125G>A

gnomAD frequency: 0.00911  dbSNP: rs2305211
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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 RCV000939925 SCV001085779 benign not provided 2022-11-29 criteria provided, single submitter clinical testing
GeneDx RCV000939925 SCV001801934 likely benign not provided 2018-07-10 criteria provided, single submitter clinical testing

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