ClinVar Miner

Submissions for variant NM_004519.4(KCNQ3):c.778-10A>G

gnomAD frequency: 0.00010  dbSNP: rs750579086
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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 RCV000868727 SCV001010093 likely benign Benign neonatal seizures 2024-10-17 criteria provided, single submitter clinical testing

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