ClinVar Miner

Submissions for variant NM_004519.4(KCNQ3):c.1467T>C (p.Asp489=)

dbSNP: rs2130942553
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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 RCV001447010 SCV001650068 likely benign Benign neonatal seizures 2023-09-11 criteria provided, single submitter clinical testing

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