ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.4806C>T (p.Tyr1602=)

dbSNP: rs2154179146
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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 RCV002162662 SCV002420674 likely benign Nemaline myopathy 2 2021-10-20 criteria provided, single submitter clinical testing

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