ClinVar Miner

Submissions for variant NM_001961.4(EEF2):c.1746G>A (p.Thr582=)

gnomAD frequency: 0.00052  dbSNP: rs148878859
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
Athena Diagnostics RCV000518665 SCV000613226 benign not specified 2024-03-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002527469 SCV003282343 likely benign not provided 2024-12-09 criteria provided, single submitter clinical testing

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