ClinVar Miner

Submissions for variant NM_152393.4(KLHL40):c.693C>T (p.Arg231=)

dbSNP: rs2125844758
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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 RCV002177975 SCV002344494 likely benign Nemaline myopathy 8 2022-06-27 criteria provided, single submitter clinical testing

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