ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.13266A>G (p.Pro4422=)

dbSNP: rs2153925623
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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 RCV001392671 SCV001594317 likely benign Nemaline myopathy 2 2023-11-24 criteria provided, single submitter clinical testing

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