ClinVar Miner

Submissions for variant NM_000335.4(SCN5A):c.885G>A (p.Glu295=) (rs373342830)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000771371 SCV000903667 likely benign Arrhythmia 2018-06-11 criteria provided, single submitter clinical testing
GeneDx RCV000127960 SCV000171547 benign not specified 2013-05-16 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.
Invitae RCV000469483 SCV000557139 likely benign Brugada syndrome 2017-12-08 criteria provided, single submitter clinical testing

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