ClinVar Miner

Submissions for variant NM_030957.4(ADAMTS10):c.*85dup

dbSNP: rs576948646
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000398934 SCV000415706 uncertain significance Weill-Marchesani syndrome 2016-06-14 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003418046 SCV004146551 uncertain significance not provided 2022-11-01 criteria provided, single submitter clinical testing

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