ClinVar Miner

Submissions for variant GRCh37/hg19 22q11.21(chr22:20030799-20068380)x1

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Pathology Laboratory,Cleveland Clinic RCV000993708 SCV000999014 uncertain significance Autistic disorder of childhood onset 2018-08-01 criteria provided, single submitter clinical testing One child with autism; variant inherited from normal mother and mat grandfather

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