ClinVar Miner

Submissions for variant NM_030957.4(ADAMTS10):c.1588-179G>T

gnomAD frequency: 0.92646  dbSNP: rs9749567
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001549065 SCV001769137 benign Weill-Marchesani syndrome 1 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001673189 SCV001889874 benign not provided 2018-06-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001673189 SCV005309139 benign not provided criteria provided, single submitter not provided

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