ClinVar Miner

Submissions for variant NM_002834.4(PTPN11):c.14+8G>T (rs886048965)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000346689 SCV000376311 uncertain significance Noonan syndrome with multiple lentigines 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000406530 SCV000376312 uncertain significance Metachondromatosis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000302391 SCV000376313 uncertain significance Noonan syndrome 2016-06-14 criteria provided, single submitter clinical testing

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