ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.4810+23C>T

gnomAD frequency: 0.00041  dbSNP: rs369559182
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breakthrough Genomics, Breakthrough Genomics RCV001730431 SCV005238195 benign not provided criteria provided, single submitter not provided
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001730431 SCV001979643 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001730432 SCV001980491 benign not specified no assertion criteria provided clinical testing

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