ClinVar Miner

Submissions for variant NM_001072.4(UGT1A6):c.862-6270C>T (rs199766420)

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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 RCV000347475 SCV000428649 uncertain significance Gilbert's syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000405057 SCV000428650 uncertain significance Lucey-Driscoll syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000312449 SCV000428651 uncertain significance Crigler-Najjar syndrome 2016-06-14 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000598199 SCV000707902 uncertain significance not provided 2018-01-29 criteria provided, single submitter clinical testing

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