ClinVar Miner

Submissions for variant NM_033056.4(PCDH15):c.4915_4918dup (p.Arg1640fs)

dbSNP: rs780945310
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000669291 SCV000794030 uncertain significance Usher syndrome type 1F 2017-11-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002060819 SCV002440612 likely benign not provided 2024-01-04 criteria provided, single submitter clinical testing

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