ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.1471-6C>T

dbSNP: rs1176788819
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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 RCV001421800 SCV001624332 likely benign Nemaline myopathy 2 2021-02-01 criteria provided, single submitter clinical testing

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