ClinVar Miner

Submissions for variant NM_000077.4(CDKN2A):c.297G>T (p.Arg99=) (rs587778191)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000571421 SCV000669218 uncertain significance Hereditary cancer-predisposing syndrome 2017-06-13 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient evidence
ITMI RCV000120546 SCV000084700 not provided not specified 2013-09-19 no assertion provided reference population

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