ClinVar Miner

Submissions for variant GRCh37/hg19 13q22.1(chr13:74152544-74283131)

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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 RCV000770942 SCV000854404 uncertain significance Aortic valve disorder 2018-11-14 no assertion criteria provided research

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