ClinVar Miner

Submissions for variant NM_139057.4(ADAMTS17):c.*1227AAGG[1]

dbSNP: rs10549565
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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 RCV000352425 SCV000389856 benign Weill-Marchesani 4 syndrome, recessive 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001672505 SCV001882151 benign not provided 2021-05-08 criteria provided, single submitter clinical testing

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