ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.6825A>T (p.Gly2275=)

gnomAD frequency: 0.00002  dbSNP: rs761057549
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000934830 SCV001080562 likely benign Nemaline myopathy 2 2023-12-04 criteria provided, single submitter clinical testing

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