ClinVar Miner

Submissions for variant NM_004519.4(KCNQ3):c.1236-20dup

dbSNP: rs754643102
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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 RCV002204081 SCV002495098 benign Benign neonatal seizures 2022-12-25 criteria provided, single submitter clinical testing

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