ClinVar Miner

Submissions for variant NM_001384140.1(PCDH15):c.297C>G (p.Thr99=)

dbSNP: rs762026724
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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 RCV000941868 SCV001087770 likely benign not provided 2023-06-16 criteria provided, single submitter clinical testing
Natera, Inc. RCV001832161 SCV002094962 likely benign Usher syndrome type 1F 2020-10-21 no assertion criteria provided clinical testing

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