ClinVar Miner

Submissions for variant NM_001384140.1(PCDH15):c.2751+8C>T

dbSNP: rs1360011079
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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 RCV001306448 SCV001495820 likely benign not provided 2024-03-17 criteria provided, single submitter clinical testing
Natera, Inc. RCV001836277 SCV002086599 uncertain significance Usher syndrome type 1F 2020-06-04 no assertion criteria provided clinical testing

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