ClinVar Miner

Submissions for variant NM_006063.3(KLHL41):c.1641T>C (p.Ile547=)

dbSNP: rs550333896
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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 RCV001411361 SCV001613423 likely benign Nemaline myopathy 9 2022-08-09 criteria provided, single submitter clinical testing

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