ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.10986C>T (p.Tyr3662=)

gnomAD frequency: 0.00004  dbSNP: rs373365702
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 RCV000871915 SCV001013649 likely benign Nemaline myopathy 2 2024-01-17 criteria provided, single submitter clinical testing
Natera, Inc. RCV000871915 SCV002077099 likely benign Nemaline myopathy 2 2020-11-06 no assertion criteria provided clinical testing

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