ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.13568G>C (p.Ser4523Thr)

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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 RCV003079062 SCV003459871 likely benign not provided 2024-12-18 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005045239 SCV005672728 uncertain significance Usher syndrome type 2C; Febrile seizures, familial, 4 2024-03-28 criteria provided, single submitter clinical testing

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