List of variants reported as likely pathogenic for Noonan syndrome by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_004333.6(BRAF):c.1802A>T (p.Lys601Ile)	rs397507484
NM_006767.4(LZTR1):c.200+1G>C
NM_006939.4(SOS2):c.1141C>G (p.Leu381Val)

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