ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.5763G>A (p.Lys1921=)

gnomAD frequency: 0.00002  dbSNP: rs760280154
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
Labcorp Genetics (formerly Invitae), Labcorp RCV005208974 SCV002392952 likely benign not provided 2024-02-17 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004002944 SCV004825371 likely benign Cardiac arrhythmia 2023-05-04 criteria provided, single submitter clinical testing

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