List of variants reported as likely pathogenic for Noonan syndrome by Center for Molecular Medicine, Children’s Hospital of Fudan University

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_002880.4(RAF1):c.61G>A (p.Val21Met)	rs752484962	0.00001
NM_006767.4(LZTR1):c.722T>C (p.Phe241Ser)	rs1423756155

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