ClinVar Miner

Submissions for variant NM_002485.4:c.703-20insA

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000160769 SCV000211428 benign Hereditary cancer-predisposing syndrome 2014-07-11 criteria provided, single submitter clinical testing The variant is found in HEREDICANCER panel(s).

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