ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.17265G>A (p.Lys5755=)

dbSNP: rs2153754655
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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 RCV001480207 SCV001684522 likely benign Nemaline myopathy 2 2019-12-02 criteria provided, single submitter clinical testing

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