ClinVar Miner

Submissions for variant NM_006922.4(SCN3A):c.363T>C (p.Ala121=)

gnomAD frequency: 0.00019  dbSNP: rs145171998
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000713082 SCV000289604 benign not provided 2025-01-30 criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000713082 SCV000708026 uncertain significance not provided 2017-05-30 criteria provided, single submitter clinical testing
Athena Diagnostics RCV004999151 SCV000843650 benign not specified 2024-07-05 criteria provided, single submitter clinical testing

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