ClinVar Miner

Submissions for variant NM_015141.4(GPD1L):c.367-4G>A

dbSNP: rs1700721746
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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 RCV001399701 SCV001601493 likely benign Brugada syndrome 2022-09-27 criteria provided, single submitter clinical testing

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