List of variants reported as benign for Noonan syndrome by Fulgent Genetics, Fulgent Genetics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_002834.5(PTPN11):c.-273G>A	rs58805176	0.10884
NM_004333.6(BRAF):c.1315-18T>G	rs6959000	0.00771
NM_005633.4(SOS1):c.1074+5G>C	rs145155424	0.00637
NM_005633.4(SOS1):c.2122G>A (p.Ala708Thr)	rs140811086	0.00282
NM_002880.4(RAF1):c.581+4A>G	rs201776526	0.00082

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