ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.*2388TA[10]

dbSNP: rs143648355
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000294757 SCV000416594 uncertain significance Mowat-Wilson syndrome 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004694477 SCV005187923 uncertain significance not provided criteria provided, single submitter not provided

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