ClinVar Miner

Submissions for variant NM_001961.4(EEF2):c.1151-7C>T

gnomAD frequency: 0.00121  dbSNP: rs200181170
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000517630 SCV000613222 benign not specified 2021-02-01 criteria provided, single submitter clinical testing
Invitae RCV000898913 SCV001043149 likely benign not provided 2023-12-21 criteria provided, single submitter clinical testing

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