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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