ClinVar Miner

Submissions for variant NM_022124.6(CDH23):c.2733+14A>C

dbSNP: rs1865637901
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003687202 SCV004430291 likely benign not provided 2023-07-03 criteria provided, single submitter clinical testing

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