ClinVar Miner

Submissions for variant NM_033056.4(PCDH15):c.5266_5319del (p.Pro1756_Pro1773del)

dbSNP: rs1554820050
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000672237 SCV000797327 uncertain significance Usher syndrome type 1F 2018-01-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002531312 SCV003466106 likely benign not provided 2023-09-10 criteria provided, single submitter clinical testing

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