ClinVar Miner

Submissions for variant NM_022124.6(CDH23):c.2121G>A (p.Glu707=)

dbSNP: rs2132705835
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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 RCV001476548 SCV001680759 likely benign not provided 2022-02-04 criteria provided, single submitter clinical testing

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