ClinVar Miner

Submissions for variant NM_000077.4(CDKN2A):c.-14C>T (rs764244718)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000579472 SCV000684500 benign Hereditary cancer-predisposing syndrome 2016-08-08 criteria provided, single submitter clinical testing
Counsyl RCV000411551 SCV000488898 uncertain significance Melanoma-pancreatic cancer syndrome 2016-07-22 criteria provided, single submitter clinical testing
GeneDx RCV000428256 SCV000512560 likely benign not specified 2017-11-29 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Invitae RCV000205775 SCV000262134 likely benign Hereditary cutaneous melanoma 2016-01-10 criteria provided, single submitter clinical testing

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