ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.1614T>C (p.His538=)

gnomAD frequency: 0.00001  dbSNP: rs769074908
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 RCV000975324 SCV001123207 likely benign Nemaline myopathy 2 2023-06-15 criteria provided, single submitter clinical testing
Natera, Inc. RCV000975324 SCV002077816 likely benign Nemaline myopathy 2 2020-11-03 no assertion criteria provided clinical testing

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