List of variants reported as benign for Multiple synostoses syndrome 3

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Total variants: 31

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HGVS	dbSNP	gnomAD frequency
NM_002010.3(FGF9):c.*9G>A	rs9509842	0.98213
NM_002010.3(FGF9):c.447A>G (p.Ser149=)	rs9509841	0.78590
NM_002010.3(FGF9):c.381+17C>T	rs2274296	0.27243
NM_002010.3(FGF9):c.278-14C>T	rs3818460	0.25974
NM_002010.3(FGF9):c.*1094C>T	rs3715	0.22949
NM_002010.3(FGF9):c.*2563G>C	rs7317625	0.20594
NM_002010.3(FGF9):c.*372A>T	rs546782	0.20354
NM_002010.3(FGF9):c.*496C>T	rs9509843	0.03191
NM_002010.3(FGF9):c.*2585C>T	rs74036838	0.01723
NM_002010.3(FGF9):c.*996A>G	rs17070748	0.00874
NM_002010.3(FGF9):c.*1877G>A	rs17070759	0.00742
NM_002010.3(FGF9):c.-429G>A	rs115025644	0.00556
NM_002010.3(FGF9):c.*2634C>T	rs190925273	0.00525
NM_002010.3(FGF9):c.-171A>G	rs149762079	0.00451
NM_002010.3(FGF9):c.*516C>A	rs73430215	0.00419
NM_002010.3(FGF9):c.*1266A>G	rs370206395	0.00192
NM_002010.3(FGF9):c.327C>T (p.Gly109=)	rs34748315	0.00151
NM_002010.3(FGF9):c.-414C>T	rs187418449	0.00146
NM_002010.3(FGF9):c.*355C>G	rs147999718	0.00096
NM_002010.3(FGF9):c.-712C>T	rs376388740	0.00075
NM_002010.3(FGF9):c.*1411T>C	rs181623879	0.00063
NM_002010.3(FGF9):c.*208G>A	rs552081915	0.00050
NM_002010.3(FGF9):c.*2325A>G	rs143740722	0.00031
NM_002010.3(FGF9):c.*318G>A	rs17070736	0.00029
NM_002010.3(FGF9):c.-726C>T	rs531745333	0.00024
NM_002010.3(FGF9):c.*1741C>T	rs376775173	0.00016
NM_002010.3(FGF9):c.*442T>C	rs573811075	0.00010
NM_002010.3(FGF9):c.*266G>A	rs557670544	0.00001
NM_002010.3(FGF9):c.*1604C>G	rs111765283
NM_002010.3(FGF9):c.*541C>A	rs17070747
NM_002010.3(FGF9):c.516G>T (p.Pro172=)	rs201876493

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