ClinVar Miner

Submissions for variant NM_033056.4(PCDH15):c.5272_5280del (p.Pro1758_Pro1760del)

dbSNP: rs754779351
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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 RCV001343043 SCV001536999 likely benign not provided 2023-06-15 criteria provided, single submitter clinical testing
Natera, Inc. RCV001825891 SCV002077656 uncertain significance Usher syndrome type 1F 2020-12-25 no assertion criteria provided clinical testing

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