ClinVar Miner

Submissions for variant NM_152393.4(KLHL40):c.1608-4C>G

dbSNP: rs2125846065
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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 RCV001471206 SCV001675308 likely benign Nemaline myopathy 8 2020-01-15 criteria provided, single submitter clinical testing

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