ClinVar Miner

Submissions for variant NC_000023.10:g.(29976475_30082636)_(31196736_31462831)del

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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 Munich, Klinikum Rechts Der Isar, TU München RCV000513432 SCV000608366 pathogenic Congenital adrenal hypoplasia, X-linked 2017-10-16 criteria provided, single submitter clinical testing

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