ClinVar Miner

Submissions for variant NM_007078.3(LDB3):c.399A>T (p.Pro133=)

dbSNP: rs769713715
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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 RCV000949140 SCV001095378 likely benign Myofibrillar myopathy 4 2023-06-13 criteria provided, single submitter clinical testing

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