ClinVar Miner

List of variants reported as uncertain significance for Vici syndrome by Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet

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Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_020964.3(EPG5):c.1871T>C (p.Leu624Pro) rs2145906621
NM_020964.3(EPG5):c.4931_4936del (p.Val1644_His1645del) rs2145491212

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