ClinVar Miner

Submissions for variant GRCh37/hg19 7q21.13-21.2(chr7:90054667-91313448)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre for Mendelian Genomics,University Medical Centre Ljubljana RCV000626539 SCV000747240 uncertain significance Autistic disorder of childhood onset; Global developmental delay; Cognitive impairment; Delayed speech and language development; Intellectual disability, moderate 2017-01-01 criteria provided, single submitter clinical testing

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