ClinVar Miner

List of variants in gene FGF9 reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 32
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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.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.-117dup rs10624265
NM_002010.3(FGF9):c.-118_-117dup rs10624265
NM_002010.3(FGF9):c.516G>T (p.Pro172=) rs201876493

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