ClinVar Miner

Submissions for variant NM_020964.3(EPG5):c.7443-621A>G

dbSNP: rs930302721
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
New York Genome Center RCV001839238 SCV002099205 uncertain significance Vici syndrome 2021-04-25 criteria provided, single submitter clinical testing

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