ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.11043G>A (p.Val3681=)

dbSNP: rs886038428
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000253829 SCV000307193 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001421301 SCV001623824 likely benign Nemaline myopathy 2 2023-11-27 criteria provided, single submitter clinical testing

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