ClinVar Miner

Submissions for variant GRCh37/hg19 15q11.2(chr15:22765628-23217514)x1

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centro Nacional de Genética Medica "Dr. Eduardo E. Castilla", Administración Nacional de Laboratorios e Institutos de Salud RCV000856647 SCV000966018 pathogenic Chromosome 15q11.2 deletion syndrome 2019-01-01 criteria provided, single submitter clinical testing

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