ClinVar Miner

Submissions for variant NM_001271208.2(NEB):c.3468C>T (p.Val1156=) (rs373258662)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000502944 SCV000595954 uncertain significance not specified 2016-06-08 criteria provided, single submitter clinical testing
Invitae RCV000641454 SCV000763095 likely benign Nemaline myopathy 2 2017-09-29 criteria provided, single submitter clinical testing

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