ClinVar Miner

Submissions for variant NM_001072.4(UGT1A6):c.1319T>C (p.Met440Thr) (rs202172337)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000378763 SCV000428661 uncertain significance Crigler-Najjar syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000270243 SCV000428662 uncertain significance Gilbert's syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000325272 SCV000428663 uncertain significance Lucey-Driscoll syndrome 2016-06-14 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000732528 SCV000860494 uncertain significance not provided 2018-03-23 criteria provided, single submitter clinical testing

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