ClinVar Miner

Submissions for variant NM_020964.3(EPG5):c.2694A>G (p.Gly898=)

dbSNP: rs2511885765
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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 RCV003655778 SCV004485861 likely benign Vici syndrome 2022-12-22 criteria provided, single submitter clinical testing

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