ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.*560del

dbSNP: rs533637050
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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 RCV000408166 SCV000416625 uncertain significance Mowat-Wilson syndrome 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004694480 SCV005187925 uncertain significance not provided criteria provided, single submitter not provided

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