ClinVar Miner

Submissions for variant NM_000814.6(GABRB3):c.183C>T (p.Val61=)

dbSNP: rs778097525
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000995280 SCV001149372 likely benign not provided 2019-01-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005213422 SCV005855633 likely benign Epilepsy, childhood absence, susceptibility to, 1; Epilepsy, childhood absence, susceptibility to, 5 2025-01-14 criteria provided, single submitter clinical testing

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