List of variants reported as likely pathogenic for Noonan syndrome by Genomic Research Center, Shahid Beheshti University of Medical Sciences

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_002834.5(PTPN11):c.959A>G (p.Asn320Ser)	rs1398859175	0.00001
NM_004333.6(BRAF):c.1387A>G (p.Ile463Val)	rs1562957000

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