ClinVar Miner

Submissions for variant GRCh37/hg19 9q34.3(chr9:140605375-140919644)x1

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics Center, Xinhua Hospital affiliated to Shanghai Jiao Tong University School of Medicine RCV004813387 SCV005438259 pathogenic Kleefstra syndrome 1 2024-11-01 no assertion criteria provided clinical testing

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