ClinVar Miner

Submissions for variant NM_006922.4(SCN3A):c.4983G>C (p.Leu1661=)

dbSNP: rs1018125027
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV001288734 SCV001476049 uncertain significance not provided 2020-11-10 criteria provided, single submitter clinical testing
Invitae RCV001288734 SCV003262960 likely benign not provided 2023-12-08 criteria provided, single submitter clinical testing

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