ClinVar Miner

Submissions for variant NM_000463.3(UGT1A1):c.1270G>T (p.Glu424Ter)

dbSNP: rs2126038122
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Gastroenterology, Ruijin Hospital, Shanghai Jiao Tong University, School of Medicine RCV002221172 SCV002498577 pathogenic Gilbert syndrome no assertion criteria provided clinical testing

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