ClinVar Miner

Submissions for variant GRCh37/hg19 15q11.2(chr15:22765628-23085096)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Medical Genetics Laboratory,CHRU Nancy RCV001291952 SCV001480565 pathogenic Autistic disorder of childhood onset; Delayed speech and language development 2020-10-01 criteria provided, single submitter clinical testing

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