ClinVar Miner

Submissions for variant NM_006922.4(SCN3A):c.991C>A (p.Gln331Lys)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003491435 SCV004237156 uncertain significance not provided 2023-10-31 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003491435 SCV005693229 likely benign not provided 2024-04-25 criteria provided, single submitter clinical testing

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