ClinVar Miner

Submissions for variant NM_007078.3(LDB3):c.846G>T (p.Thr282=)

dbSNP: rs1026972237
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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 RCV002147552 SCV002413477 likely benign Myofibrillar myopathy 4 2022-04-03 criteria provided, single submitter clinical testing

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