ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.25298-4dup

dbSNP: rs757290966
Minimum review status: Collection method:
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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 RCV002127485 SCV002402460 benign Nemaline myopathy 2 2023-04-08 criteria provided, single submitter clinical testing

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