ClinVar Miner

Submissions for variant GRCh38/hg38 Xp22.31(chrX:6570680-8129470)x1

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISCA site 17 RCV000148177 SCV000080407 pathogenic See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 4 RCV000053052 SCV000175660 pathogenic See cases 2017-09-01 no assertion criteria provided clinical testing X-linked in a male
ISCA site 1 RCV000053052 SCV000175661 benign See cases 2010-12-22 no assertion criteria provided clinical testing
ISCA site 8 RCV000053052 SCV000175663 pathogenic See cases 2010-10-20 no assertion criteria provided clinical testing

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