ClinVar Miner

Submissions for variant NC_000003.11:g.37089454_37101079del

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein RCV000022503 SCV002515988 pathogenic Colorectal cancer, hereditary nonpolyposis, type 2 2021-10-26 criteria provided, single submitter clinical testing
OMIM RCV000022503 SCV000043792 pathogenic Colorectal cancer, hereditary nonpolyposis, type 2 2011-10-01 no assertion criteria provided literature only

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