ClinVar Miner

Submissions for variant NM_004519.4(KCNQ3):c.1884+11del

dbSNP: rs749463018
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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 RCV002105889 SCV002408667 benign Benign neonatal seizures 2025-01-30 criteria provided, single submitter clinical testing

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