ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.23871A>G (p.Pro7957=)

dbSNP: rs922619160
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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 RCV001501961 SCV001706783 likely benign Nemaline myopathy 2 2022-03-18 criteria provided, single submitter clinical testing

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