ClinVar Miner

Submissions for variant NM_001384140.1(PCDH15):c.3711T>C (p.Asp1237=)

dbSNP: rs61731382
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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 RCV000978276 SCV001126204 likely benign not provided 2024-02-13 criteria provided, single submitter clinical testing
Natera, Inc. RCV001273383 SCV001456414 uncertain significance Usher syndrome type 1F 2020-02-13 no assertion criteria provided clinical testing

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