ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.7908C>T (p.Asp2636=)

gnomAD frequency: 0.00001  dbSNP: rs774348830
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000950945 SCV001097290 likely benign Nemaline myopathy 2 2024-01-29 criteria provided, single submitter clinical testing
Natera, Inc. RCV000950945 SCV001457004 likely benign Nemaline myopathy 2 2020-04-27 no assertion criteria provided clinical testing

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