ClinVar Miner

Submissions for variant NM_000815.5(GABRD):c.1194A>C (p.Thr398=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003826711 SCV004628447 likely benign Idiopathic generalized epilepsy 2023-06-18 criteria provided, single submitter clinical testing

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