ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.4540-7C>T

gnomAD frequency: 0.00002  dbSNP: rs1553693746
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
Color Diagnostics, LLC DBA Color Health RCV001843284 SCV001352747 likely benign Cardiac arrhythmia 2018-12-31 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003658782 SCV003481564 likely benign not provided 2025-01-19 criteria provided, single submitter clinical testing

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