ClinVar Miner

Submissions for variant NM_005458.8(GABBR2):c.1529+8A>G

dbSNP: rs1588135597
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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 RCV001462480 SCV001666397 likely benign Epileptic encephalopathy 2020-07-07 criteria provided, single submitter clinical testing

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