List of variants reported as likely pathogenic for Noonan syndrome by Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_002834.5(PTPN11):c.1282G>A (p.Val428Met)	rs397507536	0.00003
NM_002524.5(NRAS):c.108A>G (p.Ile36Met)	rs2101743991

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