ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.489G>A (p.Val163=)

dbSNP: rs2150759969
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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 RCV001493816 SCV001698452 likely benign Nemaline myopathy 2 2023-01-31 criteria provided, single submitter clinical testing

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