ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.3732A>G (p.Pro1244=)

dbSNP: rs1282060717
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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 RCV002098759 SCV002399661 likely benign Nemaline myopathy 2 2021-07-04 criteria provided, single submitter clinical testing

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