List of variants reported as uncertain significance for Noonan syndrome and Noonan-related syndrome by Clinical Genomics Laboratory, Stanford Medicine

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_006939.4(SOS2):c.1868G>A (p.Arg623His)	rs138459515	0.00010
NM_007373.4(SHOC2):c.355A>G (p.Ile119Val)	rs147068827	0.00009
NM_006939.4(SOS2):c.13C>G (p.Pro5Ala)	rs976486198	0.00004
NM_006939.4(SOS2):c.2350C>T (p.Arg784Cys)	rs760520078	0.00002
NM_006767.4(LZTR1):c.1735G>A (p.Val579Met)	rs765416902	0.00001
NM_005343.4(HRAS):c.11A>C (p.Tyr4Ser)	rs764622691
NM_005633.4(SOS1):c.848T>C (p.Phe283Ser)	rs1572855029

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