ClinVar Miner

Submissions for variant NM_000392.5(ABCC2):c.2743C>T (p.Arg915Cys) (rs112758556)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Praxis fuer Humangenetik Tuebingen RCV000761746 SCV000891931 likely benign not provided 2018-09-30 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000318770 SCV000333745 likely benign not specified 2015-08-13 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000274873 SCV000359793 uncertain significance Dubin-Johnson syndrome 2016-06-14 criteria provided, single submitter clinical testing

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