ClinVar Miner

Submissions for variant NM_000463.3(UGT1A1):c.1198A>C (p.Asn400His)

dbSNP: rs28934877
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000729304 SCV000856953 uncertain significance not provided 2017-09-15 criteria provided, single submitter clinical testing
Juno Genomics, Hangzhou Juno Genomics, Inc RCV004819231 SCV005440533 uncertain significance Bilirubin, serum level of, quantitative trait locus 1; Crigler-Najjar syndrome type 1; Lucey-Driscoll syndrome; Crigler-Najjar syndrome, type II; Gilbert syndrome criteria provided, single submitter clinical testing PM2_Supporting+PP3_Moderate+PM3_Supporting+PP4

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