ClinVar Miner

Submissions for variant NM_001377540.1(SLMAP):c.829-4G>A

gnomAD frequency: 0.00004  dbSNP: rs781322130
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001909032 SCV002174314 likely benign Brugada syndrome 2023-12-11 criteria provided, single submitter clinical testing

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