ClinVar Miner

List of variants in gene FGF9 studied for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 105
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HGVS dbSNP
NC_000013.11:g.21671064G>T
NM_002010.3(FGF9):c.*1030A>G
NM_002010.3(FGF9):c.*1094C>T rs3715
NM_002010.3(FGF9):c.*1186A>G
NM_002010.3(FGF9):c.*121A>C
NM_002010.3(FGF9):c.*1225T>C
NM_002010.3(FGF9):c.*124C>A rs886050045
NM_002010.3(FGF9):c.*1266A>G rs370206395
NM_002010.3(FGF9):c.*1360C>T rs564490885
NM_002010.3(FGF9):c.*1411T>C
NM_002010.3(FGF9):c.*1461T>C
NM_002010.3(FGF9):c.*1471C>T rs569079834
NM_002010.3(FGF9):c.*1507A>G rs886050057
NM_002010.3(FGF9):c.*1604C>G rs111765283
NM_002010.3(FGF9):c.*1679A>G
NM_002010.3(FGF9):c.*1741C>T rs376775173
NM_002010.3(FGF9):c.*1847G>T rs577880272
NM_002010.3(FGF9):c.*1877G>A rs17070759
NM_002010.3(FGF9):c.*1903C>T rs886050058
NM_002010.3(FGF9):c.*208G>A rs552081915
NM_002010.3(FGF9):c.*2114C>T
NM_002010.3(FGF9):c.*2186T>A rs199639996
NM_002010.3(FGF9):c.*2210del rs577984328
NM_002010.3(FGF9):c.*2256C>T
NM_002010.3(FGF9):c.*2276T>C
NM_002010.3(FGF9):c.*2291A>C
NM_002010.3(FGF9):c.*2325A>G rs143740722
NM_002010.3(FGF9):c.*2356A>C
NM_002010.3(FGF9):c.*2363A>G rs886050060
NM_002010.3(FGF9):c.*2463dup rs757466207
NM_002010.3(FGF9):c.*2469G>C
NM_002010.3(FGF9):c.*2497del rs148832636
NM_002010.3(FGF9):c.*2563G>C rs7317625
NM_002010.3(FGF9):c.*2585C>T rs74036838
NM_002010.3(FGF9):c.*2586A>G rs886050063
NM_002010.3(FGF9):c.*2594G>A
NM_002010.3(FGF9):c.*2634C>T rs190925273
NM_002010.3(FGF9):c.*266G>A rs557670544
NM_002010.3(FGF9):c.*266_*267GT[5] rs761639029
NM_002010.3(FGF9):c.*2739G>A
NM_002010.3(FGF9):c.*274A>G
NM_002010.3(FGF9):c.*274_*275del rs886050049
NM_002010.3(FGF9):c.*274_*277del rs201279299
NM_002010.3(FGF9):c.*274_*279del rs886050047
NM_002010.3(FGF9):c.*276_*277GT[14] rs61706549
NM_002010.3(FGF9):c.*276_*277GT[16] rs61706549
NM_002010.3(FGF9):c.*276_*277GT[19] rs61706549
NM_002010.3(FGF9):c.*2782A>G
NM_002010.3(FGF9):c.*2787G>T rs758942316
NM_002010.3(FGF9):c.*278G>A
NM_002010.3(FGF9):c.*2965C>T rs181292662
NM_002010.3(FGF9):c.*306A>G rs75400485
NM_002010.3(FGF9):c.*318G>A rs17070736
NM_002010.3(FGF9):c.*355C>G rs147999718
NM_002010.3(FGF9):c.*372A>T rs546782
NM_002010.3(FGF9):c.*37A>T
NM_002010.3(FGF9):c.*380C>G rs886050051
NM_002010.3(FGF9):c.*435C>T rs886050052
NM_002010.3(FGF9):c.*442T>C rs573811075
NM_002010.3(FGF9):c.*479_*482CTTA[1] rs886050053
NM_002010.3(FGF9):c.*496C>T rs9509843
NM_002010.3(FGF9):c.*516C>A rs73430215
NM_002010.3(FGF9):c.*519C>T
NM_002010.3(FGF9):c.*526A>C
NM_002010.3(FGF9):c.*541C>A
NM_002010.3(FGF9):c.*566T>A rs184771986
NM_002010.3(FGF9):c.*56C>T rs192733031
NM_002010.3(FGF9):c.*586A>T
NM_002010.3(FGF9):c.*676G>A
NM_002010.3(FGF9):c.*702G>A
NM_002010.3(FGF9):c.*713T>C rs886050054
NM_002010.3(FGF9):c.*736C>T rs886050055
NM_002010.3(FGF9):c.*737G>A rs886050056
NM_002010.3(FGF9):c.*737G>T rs886050056
NM_002010.3(FGF9):c.*996A>G rs17070748
NM_002010.3(FGF9):c.*9G>A rs9509842
NM_002010.3(FGF9):c.-116dup rs1555223891
NM_002010.3(FGF9):c.-117dup rs10624265
NM_002010.3(FGF9):c.-118_-117dup rs10624265
NM_002010.3(FGF9):c.-118_-117insC rs1555223896
NM_002010.3(FGF9):c.-151G>T rs542009378
NM_002010.3(FGF9):c.-171A>G rs149762079
NM_002010.3(FGF9):c.-256G>A rs780183885
NM_002010.3(FGF9):c.-335del rs886050042
NM_002010.3(FGF9):c.-37dup rs752566182
NM_002010.3(FGF9):c.-414C>T rs187418449
NM_002010.3(FGF9):c.-429G>A rs115025644
NM_002010.3(FGF9):c.-452A>T rs886050041
NM_002010.3(FGF9):c.-45C>T rs778769503
NM_002010.3(FGF9):c.-585dup rs886050040
NM_002010.3(FGF9):c.-703C>T rs370588961
NM_002010.3(FGF9):c.-712C>T rs376388740
NM_002010.3(FGF9):c.-726C>T rs531745333
NM_002010.3(FGF9):c.-767G>C
NM_002010.3(FGF9):c.-777G>T rs567350418
NM_002010.3(FGF9):c.-796C>T rs549054241
NM_002010.3(FGF9):c.-829C>T
NM_002010.3(FGF9):c.184A>G (p.Arg62Gly) rs1555223925
NM_002010.3(FGF9):c.278-14C>T rs3818460
NM_002010.3(FGF9):c.283C>G (p.Leu95Val) rs776951218
NM_002010.3(FGF9):c.296G>A (p.Ser99Asn) rs121918322
NM_002010.3(FGF9):c.327C>T (p.Gly109=) rs34748315
NM_002010.3(FGF9):c.420C>T (p.Phe140=)
NM_002010.3(FGF9):c.447A>G (p.Ser149=) rs9509841
NM_002010.3(FGF9):c.516G>T (p.Pro172=) rs201876493

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