ClinVar Miner

Submissions for variant NM_001165963.4(SCN1A):c.447C>T (p.Asn149=)

dbSNP: rs1484003948
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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 RCV002133600 SCV002452405 likely benign Early infantile epileptic encephalopathy with suppression bursts 2021-08-23 criteria provided, single submitter clinical testing

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