ClinVar Miner

Submissions for variant NM_006063.3(KLHL41):c.78C>G (p.Leu26=)

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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 RCV002630263 SCV002949979 likely benign Nemaline myopathy 9 2022-07-30 criteria provided, single submitter clinical testing

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