ClinVar Miner

Submissions for variant NM_000814.6(GABRB3):c.240+10C>T

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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 RCV003788202 SCV004569404 likely benign Epilepsy, childhood absence, susceptibility to, 1; Epilepsy, childhood absence, susceptibility to, 5 2023-12-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004704921 SCV005213804 likely benign not provided criteria provided, single submitter not provided

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