ClinVar Miner

Submissions for variant NM_001368067.1(LDB3):c.849C>T (p.Ser283=)

dbSNP: rs1846156972
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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 RCV001454114 SCV001657826 likely benign Myofibrillar myopathy 4 2022-12-31 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002495646 SCV002795374 likely benign Dilated cardiomyopathy 1C; Myofibrillar myopathy 4 2021-07-27 criteria provided, single submitter clinical testing

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