ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.20217C>T (p.Thr6739=)

dbSNP: rs2153617890
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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 RCV001503959 SCV001708820 likely benign Nemaline myopathy 2 2020-01-15 criteria provided, single submitter clinical testing

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