ClinVar Miner

Submissions for variant NM_004064.4(CDKN1B):c.475+5T>C (rs781394293)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000555465 SCV000646221 uncertain significance Multiple endocrine neoplasia, type 4 2017-08-09 criteria provided, single submitter clinical testing
Ambry Genetics RCV001022991 SCV001184796 uncertain significance Hereditary cancer-predisposing syndrome 2018-01-11 criteria provided, single submitter clinical testing Insufficient evidence

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