ClinVar Miner

Submissions for variant NM_033056.4(PCDH15):c.5355_5365del (p.Ile1786fs)

dbSNP: rs1554819970
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000672805 SCV000797949 uncertain significance Usher syndrome type 1F 2018-02-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003679017 SCV004407514 likely benign not provided 2022-12-13 criteria provided, single submitter clinical testing

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