ClinVar Miner

Submissions for variant NM_001037.5(SCN1B):c.591-5C>T

gnomAD frequency: 0.00003  dbSNP: rs1555721514
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000605626 SCV000729880 likely benign not specified 2017-05-17 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 RCV002064381 SCV002342907 likely benign Brugada syndrome 5 2023-10-30 criteria provided, single submitter clinical testing

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