ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.19104A>C (p.Val6368=)

dbSNP: rs1577576100
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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 RCV001402133 SCV001603977 likely benign Nemaline myopathy 2 2019-10-29 criteria provided, single submitter clinical testing

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