ClinVar Miner

Submissions for variant NM_000077.4(CDKN2A):c.150+20C>T (rs550846229)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000583339 SCV000689581 likely benign Hereditary cancer-predisposing syndrome 2017-09-08 criteria provided, single submitter clinical testing
Counsyl RCV000662891 SCV000785807 likely benign Melanoma-pancreatic cancer syndrome 2017-12-08 criteria provided, single submitter clinical testing
ITMI RCV000120547 SCV000084701 not provided not specified 2013-09-19 no assertion provided reference population

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