ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.*2525dup

dbSNP: rs886054882
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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 RCV000262514 SCV000416591 uncertain significance Mowat-Wilson syndrome 2016-06-14 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002292528 SCV002585811 likely benign not provided 2022-12-01 criteria provided, single submitter clinical testing ZEB2: BS1

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