ClinVar Miner

Submissions for variant NM_001037.5(SCN1B):c.207+19C>T

dbSNP: rs201872896
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001674681 SCV001890487 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001674681 SCV002048924 likely benign not provided 2020-10-09 criteria provided, single submitter clinical testing
Invitae RCV002032664 SCV002229340 likely benign Brugada syndrome 5 2024-02-01 criteria provided, single submitter clinical testing

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