List of variants reported as uncertain significance for Noonan syndrome by Centre for Human Genetics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_006767.4(LZTR1):c.2462T>C (p.Ile821Thr)	rs1275511136	0.00001
NM_006767.4(LZTR1):c.2426T>G (p.Leu809Arg)
NM_006767.4(LZTR1):c.851G>A (p.Arg284His)	rs768361273

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