ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.10393A>G (p.Ile3465Val)

dbSNP: rs535926481
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001240080 SCV001413002 benign Nemaline myopathy 2 2024-01-22 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003130214 SCV003812821 uncertain significance not provided 2020-11-09 criteria provided, single submitter clinical testing
Natera, Inc. RCV001240080 SCV002077119 uncertain significance Nemaline myopathy 2 2020-06-04 no assertion criteria provided clinical testing

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