ClinVar Miner

Submissions for variant NM_002834.4(PTPN11):c.332+17T>G (rs115658366)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000033486 SCV000057391 poly Rasopathy criteria provided, single submitter clinical testing Converted during submission to Benign.
Greenwood Genetic Center Diagnostic Laboratories,Greenwood Genetic Center RCV000157684 SCV000207665 benign not specified 2015-01-15 no assertion criteria provided clinical testing

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