ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.4122T>C (p.Tyr1374=)

gnomAD frequency: 0.00001  dbSNP: rs778135952
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001439914 SCV001642817 likely benign Nemaline myopathy 2 2023-06-09 criteria provided, single submitter clinical testing

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