ClinVar Miner

Submissions for variant GRCh37/hg19 Xp22.33(chrX:498249-681607)x3

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Goettingen RCV001004816 SCV001164309 uncertain significance Autistic behavior; Seizure 2019-07-02 no assertion criteria provided clinical testing

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