ClinVar Miner

Submissions for variant GRCh37/hg19 Xq26.3(chrX:135730386-135732556)x0

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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 RCV003887802 SCV004704471 pathogenic not provided 2024-02-01 criteria provided, single submitter clinical testing

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