ClinVar Miner

Submissions for variant NM_000244.3(MEN1):c.799-19TC[2] (rs764290037)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000182400 SCV000234743 benign not specified 2013-06-12 criteria provided, single submitter clinical testing The variant is found in MEN1 panel(s).
Counsyl RCV000409712 SCV000488118 uncertain significance Multiple endocrine neoplasia, type 1 2015-12-30 criteria provided, single submitter clinical testing

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