ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.3898del (p.Ser1300fs)

dbSNP: rs2061270021
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Laboratory, BC Children's and BC Women's Hospitals RCV001175240 SCV001338810 likely pathogenic Brugada syndrome 2019-04-10 no assertion criteria provided clinical testing

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