ClinVar Miner

Submissions for variant NM_003392.7(WNT5A):c.*1952_*1953del

dbSNP: rs78756487
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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 RCV000277253 SCV000445619 uncertain significance Autosomal dominant Robinow syndrome 1 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001683379 SCV001904147 benign not provided 2021-05-17 criteria provided, single submitter clinical testing

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