List of variants reported as pathogenic for Noonan syndrome 3 by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_002834.5(PTPN11):c.188A>G (p.Tyr63Cys)	rs121918459	0.00001
NM_002834.5(PTPN11):c.1528C>G (p.Gln510Glu)	rs397507549
NM_002834.5(PTPN11):c.1529A>C (p.Gln510Pro)	rs121918470
NM_002834.5(PTPN11):c.174C>A (p.Asn58Lys)	rs397507506
NM_002834.5(PTPN11):c.181G>A (p.Asp61Asn)	rs397507510
NM_002834.5(PTPN11):c.181G>C (p.Asp61His)	rs397507510
NM_002834.5(PTPN11):c.215C>G (p.Ala72Gly)	rs121918454
NM_002834.5(PTPN11):c.236A>G (p.Gln79Arg)	rs121918466
NM_002834.5(PTPN11):c.417G>C (p.Glu139Asp)	rs397507520
NM_002834.5(PTPN11):c.853T>C (p.Phe285Leu)	rs397507531
NM_002834.5(PTPN11):c.855T>G (p.Phe285Leu)	rs397516810
NM_002834.5(PTPN11):c.923A>G (p.Asn308Ser)	rs121918455
NM_004985.5(KRAS):c.40G>A (p.Val14Ile)	rs104894365
NM_005633.4(SOS1):c.1655G>A (p.Arg552Lys)	rs397517154

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