List of variants reported as uncertain significance for Noonan syndrome by Molecular Genetics, Royal Melbourne Hospital

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_006939.4(SOS2):c.1208G>C (p.Cys403Ser)	rs201821194	0.00002
NM_004333.6(BRAF):c.1056T>A (p.Asp352Glu)	rs1398817791

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