ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.13206C>T (p.Ser4402=)

dbSNP: rs2153930427
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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 RCV001403971 SCV001605859 likely benign Nemaline myopathy 2 2023-05-18 criteria provided, single submitter clinical testing

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