ClinVar Miner

Submissions for variant NM_004519.4(KCNQ3):c.1569-14A>G

gnomAD frequency: 0.00001  dbSNP: rs761057466
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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 RCV002096361 SCV002396167 likely benign Benign neonatal seizures 2024-01-08 criteria provided, single submitter clinical testing

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