ClinVar Miner

Submissions for variant NM_002834.4(PTPN11):c.1599+33A>G (rs727505380)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000156978 SCV000206700 benign Noonan syndrome 2011-07-13 no assertion criteria provided clinical testing

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