ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.13368+6A>G

dbSNP: rs886038433
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000244633 SCV000307211 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000543007 SCV000640556 uncertain significance Nemaline myopathy 2 2017-09-29 criteria provided, single submitter clinical testing
GeneDx RCV001697690 SCV000731106 likely benign not provided 2020-10-26 criteria provided, single submitter clinical testing
Natera, Inc. RCV000543007 SCV001456746 uncertain significance Nemaline myopathy 2 2020-01-17 no assertion criteria provided clinical testing

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