ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.19608C>T (p.Val6536=)

dbSNP: rs1483543704
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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 RCV002105939 SCV002402100 likely benign Nemaline myopathy 2 2022-07-05 criteria provided, single submitter clinical testing

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