ClinVar Miner

Submissions for variant NM_001072.4(UGT1A6):c.1119T>C (p.Gly373=) (rs139698110)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000178105 SCV000230100 uncertain significance not provided 2018-02-20 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000359133 SCV000428658 uncertain significance Crigler-Najjar syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000264419 SCV000428659 uncertain significance Lucey-Driscoll syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000324135 SCV000428660 uncertain significance Gilbert's syndrome 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000178105 SCV001038531 likely benign not provided 2018-07-06 criteria provided, single submitter clinical testing

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