ClinVar Miner

Submissions for variant NM_022124.6(CDH23):c.6142C>T (p.Leu2048=)

dbSNP: rs1454461173
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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 RCV002203446 SCV002486482 likely benign not provided 2022-08-08 criteria provided, single submitter clinical testing

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