ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.25368G>A (p.Thr8456=)

gnomAD frequency: 0.00006  dbSNP: rs200083849
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 RCV000877586 SCV001020335 likely benign Nemaline myopathy 2 2024-01-24 criteria provided, single submitter clinical testing
Natera, Inc. RCV000877586 SCV001454421 uncertain significance Nemaline myopathy 2 2020-03-11 no assertion criteria provided clinical testing

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