ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.2024-5C>T

gnomAD frequency: 0.00001  dbSNP: rs765875042
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003657098 SCV001627949 likely benign not provided 2022-07-19 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004006960 SCV004825887 likely benign Cardiac arrhythmia 2024-01-03 criteria provided, single submitter clinical testing

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