ClinVar Miner

Submissions for variant NM_014243.3(ADAMTS3):c.2179+21G>A

gnomAD frequency: 0.98931  dbSNP: rs10024487
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001549242 SCV001769361 benign Hennekam lymphangiectasia-lymphedema syndrome 3 2021-07-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004716773 SCV005297959 benign not provided criteria provided, single submitter not provided

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