ClinVar Miner

Submissions for variant NM_001961.4(EEF2):c.627C>T (p.Leu209=)

gnomAD frequency: 0.00010  dbSNP: rs145155508
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV000518254 SCV000613237 likely benign not specified 2017-02-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000879496 SCV001022532 benign not provided 2022-11-03 criteria provided, single submitter clinical testing

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