ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.1005T>C (p.Cys335=)

gnomAD frequency: 0.00001  dbSNP: rs746053691
Minimum review status: Collection method:
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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 RCV001841124 SCV001358433 likely benign Cardiac arrhythmia 2019-11-16 criteria provided, single submitter clinical testing
Invitae RCV003657772 SCV002399722 likely benign not provided 2022-08-31 criteria provided, single submitter clinical testing

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