ClinVar Miner

Submissions for variant NM_007294.3:c.134+19insT

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000159857 SCV000209901 benign Familial cancer of breast 2014-07-08 criteria provided, single submitter clinical testing The variant is found in BRCA panel(s).

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