ClinVar Miner

Submissions for variant NM_000814.6(GABRB3):c.207C>A (p.Ile69=)

dbSNP: rs770214111
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001405153 SCV001607070 likely benign Epilepsy, childhood absence, susceptibility to, 1; Epilepsy, childhood absence, susceptibility to, 5 2018-09-26 criteria provided, single submitter clinical testing

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