ClinVar Miner

Submissions for variant GRCh37/hg19 Xp21.2-21.1(chrX:31453403-31560484)x3

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Biotechnology, Institute of Molecular and Cell Biology, University of Tartu RCV000225261 SCV000212496 benign Premature ovarian failure 2015-01-07 criteria provided, single submitter reference population

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