List of variants reported as uncertain significance for Noonan syndrome with multiple lentigines

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_002834.5(PTPN11):c.*2731G>A	rs768622106	0.00013
NM_002834.5(PTPN11):c.*1157ATG[13]	rs80269561
NM_002834.5(PTPN11):c.*1157ATG[16]	rs80269561
NM_002834.5(PTPN11):c.*1157ATG[17]	rs80269561
NM_002834.5(PTPN11):c.41_46del	rs886048967
NM_002834.5(PTPN11):c.*656del	rs886048968
NM_002880.3(RAF1):c.-340_-339GA[1]	rs527774250
NM_002880.4(RAF1):c.*729AACA[4]	rs371820097
NM_002880.4(RAF1):c.*729AACA[6]	rs371820097
NM_004333.6(BRAF):c.2128-16_2128-15del	rs886062015
NM_004333.6(BRAF):c.2128-27_2128-16delinsTCT	rs886062016
NM_004333.6(BRAF):c.2128-28dup	rs60814637
NM_004333.6(BRAF):c.2128-4del	rs886062014
NM_004333.6(BRAF):c.2128-5dup	rs373442098
NM_030662.4(MAP2K2):c.183A>T (p.Lys61Asn)	rs886041310
NM_030662.4(MAP2K2):c.692G>T (p.Arg231Leu)	rs730880511

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