ClinVar Miner

Submissions for variant NC_000019.10:g.41983952_42247520del

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Wilkie Group, Clinical Genetics Lab, WIMM, University of Oxford RCV001374687 SCV001571605 pathogenic Syndromic intellectual disability 2021-01-01 no assertion criteria provided clinical testing

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