ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.19626+10T>C

dbSNP: rs2153659730
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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 RCV001482158 SCV001686519 likely benign Nemaline myopathy 2 2020-10-16 criteria provided, single submitter clinical testing

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