ClinVar Miner

Submissions for variant NM_020964.3(EPG5):c.6622-22_6622-7dup

dbSNP: rs11333207
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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 RCV002943728 SCV003278239 likely benign Vici syndrome 2024-02-05 criteria provided, single submitter clinical testing

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