ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.3508+12G>A

dbSNP: rs587781164
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000127978 SCV000171567 benign not specified 2014-04-07 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Labcorp Genetics (formerly Invitae), Labcorp RCV003546476 SCV004274944 likely benign not provided 2023-12-30 criteria provided, single submitter clinical testing

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