ClinVar Miner

Submissions for variant GRCh37/hg19 Xp21.1(chrX:32662249-32663269)x3

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003457633 SCV004184967 likely pathogenic not provided 2023-11-01 criteria provided, single submitter clinical testing

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