ClinVar Miner

List of variants reported as likely benign for Noonan syndrome by ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories

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Total variants: 5
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NM_002834.5(PTPN11):c.1620C>T (p.His540=) rs587781132
NM_002834.5(PTPN11):c.933+25T>C rs727505386
NM_005633.4(SOS1):c.2511-13_2511-9del rs727503436
NM_005633.4(SOS1):c.3391+7A>G rs201982464
NM_005633.4(SOS1):c.396A>T (p.Ala132=) rs727505385

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