ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.423T>G (p.Gly141=)

dbSNP: rs759036441
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001491753 SCV001696355 likely benign Nemaline myopathy 2 2020-08-20 criteria provided, single submitter clinical testing

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