ClinVar Miner

Submissions for variant NM_001368067.1(LDB3):c.798A>G (p.Lys266=)

gnomAD frequency: 0.00001  dbSNP: rs370682028
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 RCV001363342 SCV001559449 likely benign Myofibrillar myopathy 4 2024-09-05 criteria provided, single submitter clinical testing

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