ClinVar Miner

Submissions for variant GRCh37/hg19 Xp22.33(chrX:2766830-2920785)x2

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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 RCV001251055 SCV001426458 uncertain significance Hypoplastic left heart syndrome 2020-04-08 no assertion criteria provided clinical testing

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