ClinVar Miner

Submissions for variant GRCh37/hg19 9p24.3-22.1(chr9:204193-18654812)

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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 RCV001352660 SCV001547228 pathogenic Trigonocephaly 2021-03-15 criteria provided, single submitter clinical testing

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