ClinVar Miner

Submissions for variant NM_007078.3(LDB3):c.1231+14C>G

gnomAD frequency: 0.00001  dbSNP: rs1846586366
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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 RCV002078547 SCV002380021 likely benign Myofibrillar myopathy 4 2021-05-19 criteria provided, single submitter clinical testing

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