ClinVar Miner

Submissions for variant NM_002834.5(PTPN11):c.1600-95C>T

gnomAD frequency: 0.37076  dbSNP: rs3741983
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001642533 SCV001860504 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000157011 SCV000206738 benign Noonan syndrome 2014-05-29 no assertion criteria provided clinical testing

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