ClinVar Miner

Submissions for variant GRCh37/hg19 11p11.2(chr11:47997461-48142707)x3

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Goettingen RCV001250257 SCV001424559 uncertain significance Aortic valve stenosis 2019-07-18 no assertion criteria provided clinical testing

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