ClinVar Miner

Submissions for variant NM_000314.7(PTEN):c.-662_-651del (rs786204880)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000169821 SCV000222141 benign Hereditary cancer-predisposing syndrome 2014-03-25 criteria provided, single submitter clinical testing aka c.-663_-652delGCAGCGGCGGCG [hg 19]. The variant is found in BR-OV-HEREDIC panel(s).

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