ClinVar Miner

Submissions for variant GRCh37/hg19 19p13.2(chr19:8213468-8227432)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre of Medical Genetics, University of Antwerp RCV000770945 SCV000854407 uncertain significance Aortic valve disease 1 2018-11-14 no assertion criteria provided research

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