ClinVar Miner

Submissions for variant NM_033056.4(PCDH15):c.4792C>T (p.Gln1598Ter)

dbSNP: rs1554820663
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000665772 SCV000789943 uncertain significance Usher syndrome type 1F 2017-03-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002530665 SCV003311541 likely benign not provided 2022-07-14 criteria provided, single submitter clinical testing

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