ClinVar Miner

Submissions for variant GRCh37/hg19 5q22.2(chr5:112155123-112174165)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 RCV002279742 SCV002098071 pathogenic Familial adenomatous polyposis due to 5q22.2 microdeletion 2022-02-02 criteria provided, single submitter clinical testing

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