ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.10101T>C (p.Asn3367=)

dbSNP: rs755069446
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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 RCV002184191 SCV002488243 likely benign Nemaline myopathy 2 2021-05-10 criteria provided, single submitter clinical testing

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