ClinVar Miner

Submissions for variant NM_001377540.1(SLMAP):c.1360+20_1360+21del

dbSNP: rs772418049
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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 RCV002206662 SCV002494136 likely benign Brugada syndrome 2022-01-12 criteria provided, single submitter clinical testing

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