ClinVar Miner

Submissions for variant NM_015141.4(GPD1L):c.619-9C>A

dbSNP: rs2044880
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001344855 SCV001538937 likely benign Brugada syndrome 2024-08-18 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002486400 SCV002790568 uncertain significance Brugada syndrome 2 2021-07-05 criteria provided, single submitter clinical testing

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