ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.15899C>G (p.Thr5300Ser)

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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 RCV002720504 SCV002991350 likely benign not provided 2024-02-01 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005044942 SCV005672734 uncertain significance Usher syndrome type 2C; Febrile seizures, familial, 4 2024-04-04 criteria provided, single submitter clinical testing

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