ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.19857T>C (p.Tyr6619=)

dbSNP: rs2153648002
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001396181 SCV001597906 likely benign Nemaline myopathy 2 2021-07-26 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003132495 SCV003810174 uncertain significance not provided 2019-09-09 criteria provided, single submitter clinical testing

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