List of variants reported as uncertain significance for Noonan syndrome by Genetics and Molecular Pathology, SA Pathology

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_006767.4(LZTR1):c.361C>T (p.His121Tyr)	rs1569154492	0.00001
NM_005633.4(SOS1):c.2764A>G (p.Ile922Val)	rs780420674
NM_006767.4(LZTR1):c.1700G>A (p.Arg567His)	rs372417941

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