ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.20263-7dup

dbSNP: rs763008896
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000556159 SCV000640660 benign Nemaline myopathy 2 2024-12-26 criteria provided, single submitter clinical testing
Athena Diagnostics RCV003482281 SCV004229801 likely benign not provided 2023-07-13 criteria provided, single submitter clinical testing

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