ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.1653G>C (p.Ala551=)

dbSNP: rs397517952
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003766986 SCV000637085 likely benign not provided 2024-07-13 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001841458 SCV001339893 likely benign Cardiac arrhythmia 2019-05-13 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV001841458 SCV004817136 likely benign Cardiac arrhythmia 2023-10-27 criteria provided, single submitter clinical testing

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