ClinVar Miner

Submissions for variant GRCh37/hg19 Xq28(chrX:153588672-153609996)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre for Mendelian Genomics, University Medical Centre Ljubljana RCV000626555 SCV000747256 pathogenic Migraine with aura 2017-01-01 criteria provided, single submitter clinical testing

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