ClinVar Miner

Submissions for variant NM_000814.6(GABRB3):c.880C>T (p.Arg294Trp)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Leipzig Medical Center RCV004759518 SCV005368111 uncertain significance Epilepsy, childhood absence, susceptibility to, 5 2022-03-29 criteria provided, single submitter clinical testing

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