ClinVar Miner

Submissions for variant NM_007078.3(LDB3):c.1587A>G (p.Pro529=)

dbSNP: rs2132482785
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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 RCV001485394 SCV001689829 likely benign Myofibrillar myopathy 4 2022-03-09 criteria provided, single submitter clinical testing

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