ClinVar Miner

Submissions for variant NM_006922.4(SCN3A):c.1773T>C (p.Asn591=)

gnomAD frequency: 0.00002  dbSNP: rs76144052
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) RCV000403613 SCV000343868 uncertain significance not provided 2016-07-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000403613 SCV001013851 likely benign not provided 2025-01-13 criteria provided, single submitter clinical testing

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