ClinVar Miner

List of variants in gene FGF9 reported as uncertain significance for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 67
Download table as spreadsheet
HGVS dbSNP
NC_000013.11:g.21671064G>T
NM_002010.3(FGF9):c.*1030A>G
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.*1360C>T rs564490885
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.*1679A>G
NM_002010.3(FGF9):c.*1847G>T rs577880272
NM_002010.3(FGF9):c.*1903C>T rs886050058
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.*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.*2586A>G rs886050063
NM_002010.3(FGF9):c.*2594G>A
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.*37A>T
NM_002010.3(FGF9):c.*380C>G rs886050051
NM_002010.3(FGF9):c.*435C>T rs886050052
NM_002010.3(FGF9):c.*479_*482CTTA[1] rs886050053
NM_002010.3(FGF9):c.*519C>T
NM_002010.3(FGF9):c.*526A>C
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.-116dup rs1555223891
NM_002010.3(FGF9):c.-151G>T rs542009378
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.-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.-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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.