ClinVar Miner

Submissions for variant NM_198271.5(LMOD3):c.1155G>T (p.Val385=)

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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 RCV005202865 SCV005833502 likely benign Nemaline myopathy 10 2024-04-13 criteria provided, single submitter clinical testing

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