List of variants reported as likely pathogenic for Noonan syndrome and Noonan-related syndrome by Tartaglia Lab, Genetics and Rare Diseases Research Division, Bambino Gesu' Children's Hospital

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_007373.4(SHOC2):c.157G>A (p.Gly53Arg)	rs2134121169
NM_007373.4(SHOC2):c.517A>G (p.Met173Val)	rs1057518206
NM_007373.4(SHOC2):c.806A>G (p.Gln269Arg)	rs864309599

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