ClinVar Miner

Submissions for variant NM_002834.4(PTPN11):c.*1006del (rs146940557)

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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 RCV000349825 SCV000376368 likely benign Noonan syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000387928 SCV000376369 likely benign Metachondromatosis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000296025 SCV000376370 likely benign Noonan syndrome with multiple lentigines 2016-06-14 criteria provided, single submitter clinical testing

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