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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