ClinVar Miner

Submissions for variant NC_000019.10:g.42227530_42259211del

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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 RCV001374688 SCV001571606 pathogenic Macrocephaly 2021-01-01 no assertion criteria provided clinical testing

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