ClinVar Miner

Submissions for variant NM_198271.5(LMOD3):c.426A>G (p.Glu142=)

dbSNP: rs111848977
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000548929 SCV000655507 benign Nemaline myopathy 10 2025-01-23 criteria provided, single submitter clinical testing
GeneDx RCV001577394 SCV001804756 likely benign not provided 2021-03-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001577394 SCV005264078 likely benign not provided criteria provided, single submitter not provided

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