ClinVar Miner

Submissions for variant NM_001037.5(SCN1B):c.40+15G>A

dbSNP: rs72556351
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000828554 SCV000970247 likely benign not provided 2018-03-13 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 RCV003509613 SCV004344696 likely benign Brugada syndrome 5 2023-09-08 criteria provided, single submitter clinical testing

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