List of variants reported as uncertain significance for Noonan syndrome and Noonan-related syndrome by Mendelics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_005633.4(SOS1):c.233T>G (p.Phe78Cys)	rs201352584	0.00019
NM_005633.4(SOS1):c.1490G>A (p.Arg497Gln)	rs371314838	0.00004
NM_002880.4(RAF1):c.226A>G (p.Met76Val)	rs730880999
NM_005633.4(SOS1):c.1727G>T (p.Arg576Ile)	rs1553356023

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