ClinVar Miner

Submissions for variant NM_001072.4(UGT1A6):c.993+15T>C (rs4148327)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000147907 SCV000195398 uncertain significance Hyperbilirubinemia 2013-03-04 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000354615 SCV000428655 likely benign Lucey-Driscoll syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000263302 SCV000428656 likely benign Gilbert's syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000299727 SCV000428657 likely benign Crigler-Najjar syndrome 2016-06-14 criteria provided, single submitter clinical testing

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