ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.3267A>G (p.Lys1089=)

dbSNP: rs2148501395
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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 RCV002159961 SCV002413509 likely benign Nemaline myopathy 2 2021-09-17 criteria provided, single submitter clinical testing

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