ClinVar Miner

Submissions for variant NM_152393.4(KLHL40):c.1086C>T (p.Phe362=)

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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 RCV003841178 SCV004694619 likely benign Nemaline myopathy 8 2023-06-10 criteria provided, single submitter clinical testing

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