ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.3416+7A>G

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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 RCV002627262 SCV002972523 likely benign not provided 2023-10-29 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005042932 SCV005666282 uncertain significance Usher syndrome type 2C; Febrile seizures, familial, 4 2024-04-04 criteria provided, single submitter clinical testing

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