ClinVar Miner

Submissions for variant NM_000335.5(SCN5A):c.3821A>G (p.Asp1274Gly)

dbSNP: rs2125849528
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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 RCV001787292 SCV002029157 likely pathogenic Brugada syndrome 2021-08-16 no assertion criteria provided clinical testing

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