List of variants reported as likely pathogenic for Noonan syndrome by Yale Center for Mendelian Genomics, Yale University

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_006939.4(SOS2):c.1126A>T (p.Thr376Ser)	rs1594982548
NM_006939.4(SOS2):c.1127C>G (p.Thr376Ser)	rs869320687
NM_006939.4(SOS2):c.791C>A (p.Thr264Lys)

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