List of variants reported as pathogenic for Noonan syndrome by Institute for Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_006767.4(LZTR1):c.993+1G>A	rs770368435	0.00001
NM_002834.5(PTPN11):c.124A>G (p.Thr42Ala)	rs397507501
NM_005633.4(SOS1):c.508A>G (p.Lys170Glu)	rs397517172

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