ClinVar Miner

Submissions for variant NM_006922.4(SCN3A):c.1617C>T (p.Phe539=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002979396 SCV003290962 benign not provided 2022-08-27 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002979396 SCV004011216 likely benign not provided 2023-04-01 criteria provided, single submitter clinical testing SCN3A: BP4, BP7

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