ClinVar Miner

Submissions for variant GRCh37/hg19 22q13.33(chr22:51123491-51219009)

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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 RCV001352662 SCV001547230 pathogenic Autistic disorder of childhood onset; Global developmental delay 2021-03-15 criteria provided, single submitter clinical testing

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