ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.19623C>T (p.Ser6541=)

dbSNP: rs2095477737
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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 RCV002138558 SCV002451111 likely benign Nemaline myopathy 2 2023-06-11 criteria provided, single submitter clinical testing

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