ClinVar Miner

Submissions for variant NM_022124.6(CDH23):c.7873-4A>G

dbSNP: rs1047300881
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003688935 SCV004429943 likely benign not provided 2023-12-14 criteria provided, single submitter clinical testing
Natera, Inc. RCV001279065 SCV001466126 uncertain significance Usher syndrome type 1 2020-09-04 no assertion criteria provided clinical testing

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