ClinVar Miner

Submissions for variant NM_001368067.1(LDB3):c.432C>T (p.Gly144=)

gnomAD frequency: 0.00002  dbSNP: rs558590519
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001467642 SCV001671669 likely benign Myofibrillar myopathy 4 2023-04-20 criteria provided, single submitter clinical testing

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