ClinVar Miner

Submissions for variant NM_001377540.1(SLMAP):c.828+11C>A

gnomAD frequency: 0.19942  dbSNP: rs2306056
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000252439 SCV000311721 benign not specified criteria provided, single submitter clinical testing
Phosphorus, Inc. RCV000577982 SCV000679921 benign Brugada syndrome 2017-08-01 criteria provided, single submitter clinical testing
GeneDx RCV001640544 SCV001856354 benign not provided 2019-03-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000577982 SCV002348693 benign Brugada syndrome 2025-02-03 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000252439 SCV005185804 benign not specified 2024-05-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001640544 SCV005300351 benign not provided criteria provided, single submitter not provided

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