ClinVar Miner

Submissions for variant NM_006922.4(SCN3A):c.2121C>T (p.Ser707=)

gnomAD frequency: 0.00025  dbSNP: rs370351101
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000729431 SCV000857094 uncertain significance not provided 2017-10-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000729431 SCV001050972 likely benign not provided 2025-01-22 criteria provided, single submitter clinical testing

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