ClinVar Miner

Submissions for variant NM_033056.4(PCDH15):c.5406G>T (p.Thr1802=)

dbSNP: rs534255804
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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 RCV000977649 SCV001125568 likely benign not provided 2023-07-31 criteria provided, single submitter clinical testing
Natera, Inc. RCV001832251 SCV002082140 likely benign Usher syndrome type 1F 2021-03-02 no assertion criteria provided clinical testing

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