ClinVar Miner

Submissions for variant NM_033056.4(PCDH15):c.5669_5671del (p.Ala1890del)

dbSNP: rs771643291
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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 RCV002537760 SCV002947563 likely benign not provided 2023-02-03 criteria provided, single submitter clinical testing
Natera, Inc. RCV001277665 SCV001464629 uncertain significance Usher syndrome type 1F 2020-04-13 no assertion criteria provided clinical testing

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