ClinVar Miner

Submissions for variant NM_002834.4(PTPN11):c.15-38C>T (rs727505378)

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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	RCV000156972	SCV000206694	benign	Noonan syndrome	2010-09-23	no assertion criteria provided	clinical testing

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