ClinVar Miner

Submissions for variant NM_152393.4(KLHL40):c.879G>A (p.Glu293=)

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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 RCV002616777 SCV003508630 likely benign Nemaline myopathy 8 2022-08-17 criteria provided, single submitter clinical testing

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