ClinVar Miner

Submissions for variant NM_004519.4(KCNQ3):c.2100C>T (p.His700=)

dbSNP: rs563382297
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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 RCV001455950 SCV001659721 likely benign Benign neonatal seizures 2023-07-17 criteria provided, single submitter clinical testing

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