ClinVar Miner

List of variants in gene FGF9 studied for congenital limb malformation

Included ClinVar conditions (336):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 108
Download table as spreadsheet
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.*274A>G rs9796160 0.02722
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.-118_-117insC rs1555223896 0.00456
NM_002010.3(FGF9):c.-171A>G rs149762079 0.00451
NM_002010.3(FGF9):c.*306A>G rs75400485 0.00431
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.*526A>C rs538980565 0.00136
NM_002010.3(FGF9):c.*355C>G rs147999718 0.00096
NM_002010.3(FGF9):c.*2291A>C rs545346016 0.00083
NM_002010.3(FGF9):c.-712C>T rs376388740 0.00075
NM_002010.3(FGF9):c.*2787G>T rs758942316 0.00073
NM_002010.3(FGF9):c.*1411T>C rs181623879 0.00063
NM_002010.3(FGF9):c.*1471C>T rs569079834 0.00063
NM_002010.3(FGF9):c.*208G>A rs552081915 0.00050
NM_002010.3(FGF9):c.*56C>T rs192733031 0.00048
NM_002010.3(FGF9):c.-37dup rs752566182 0.00032
NM_002010.3(FGF9):c.-777G>T rs567350418 0.00032
NM_002010.3(FGF9):c.*2325A>G rs143740722 0.00031
NM_002010.3(FGF9):c.*1360C>T rs564490885 0.00029
NM_002010.3(FGF9):c.*318G>A rs17070736 0.00029
NM_002010.3(FGF9):c.*435C>T rs886050052 0.00029
NM_002010.3(FGF9):c.*2965C>T rs181292662 0.00024
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.-703C>T rs370588961 0.00016
NM_002010.3(FGF9):c.*736C>T rs886050055 0.00015
NM_002010.3(FGF9):c.*2782A>G rs769128413 0.00014
NM_002010.3(FGF9):c.*442T>C rs573811075 0.00010
NM_002010.3(FGF9):c.*1679A>G rs762284852 0.00009
NM_002010.3(FGF9):c.*2356A>C rs374249081 0.00007
NM_002010.3(FGF9):c.*1903C>T rs886050058 0.00006
NM_002010.3(FGF9):c.*2186T>A rs199639996 0.00006
NM_002010.3(FGF9):c.*566T>A rs184771986 0.00006
NM_002010.3(FGF9):c.*737G>A rs886050056 0.00006
NM_002010.3(FGF9):c.420C>T (p.Phe140=) rs765041263 0.00006
NM_002010.3(FGF9):c.*519C>T rs947805508 0.00004
NM_002010.3(FGF9):c.*586A>T rs1366387106 0.00004
NM_002010.3(FGF9):c.*124C>A rs886050045 0.00003
NM_002010.3(FGF9):c.-256G>A rs780183885 0.00003
NM_002010.3(FGF9):c.283C>G (p.Leu95Val) rs776951218 0.00003
NM_002010.3(FGF9):c.*1186A>G rs1000898581 0.00002
NM_002010.3(FGF9):c.*1225T>C rs537888875 0.00002
NM_002010.3(FGF9):c.*2114C>T rs892010832 0.00002
NM_002010.3(FGF9):c.*702G>A rs983063697 0.00002
NM_002010.3(FGF9):c.*121A>C rs1168164095 0.00001
NM_002010.3(FGF9):c.*1847G>T rs577880272 0.00001
NM_002010.3(FGF9):c.*2586A>G rs886050063 0.00001
NM_002010.3(FGF9):c.*2594G>A rs919808404 0.00001
NM_002010.3(FGF9):c.*266G>A rs557670544 0.00001
NM_002010.3(FGF9):c.*2739G>A rs938753704 0.00001
NM_002010.3(FGF9):c.*380C>G rs886050051 0.00001
NM_002010.3(FGF9):c.*676G>A rs1872564551 0.00001
NM_002010.3(FGF9):c.-116dup rs1555223891 0.00001
NM_002010.3(FGF9):c.-45C>T rs778769503 0.00001
NM_002010.3(FGF9):c.-829C>T rs1871749772 0.00001
NM_002010.2(FGF9):c.-849G>T rs1871749140
NM_002010.3(FGF9):c.*1030A>G rs1872572012
NM_002010.3(FGF9):c.*1461T>C rs1872579132
NM_002010.3(FGF9):c.*1507A>G rs886050057
NM_002010.3(FGF9):c.*1604C>G rs111765283
NM_002010.3(FGF9):c.*2210del rs577984328
NM_002010.3(FGF9):c.*2256C>T rs1872594410
NM_002010.3(FGF9):c.*2276T>C rs1340564951
NM_002010.3(FGF9):c.*2363A>G rs886050060
NM_002010.3(FGF9):c.*2463dup rs757466207
NM_002010.3(FGF9):c.*2469G>C rs1371588292
NM_002010.3(FGF9):c.*2497del rs148832636
NM_002010.3(FGF9):c.*266GT[5] rs761639029
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.*276GT[14] rs61706549
NM_002010.3(FGF9):c.*276GT[16] rs61706549
NM_002010.3(FGF9):c.*276GT[19] rs61706549
NM_002010.3(FGF9):c.*278G>A rs1872549246
NM_002010.3(FGF9):c.*37A>T rs767958078
NM_002010.3(FGF9):c.*479CTTA[1] rs886050053
NM_002010.3(FGF9):c.*541C>A rs17070747
NM_002010.3(FGF9):c.*713T>C rs886050054
NM_002010.3(FGF9):c.*737G>T rs886050056
NM_002010.3(FGF9):c.-117dup rs10624265
NM_002010.3(FGF9):c.-118_-117dup rs10624265
NM_002010.3(FGF9):c.-151G>T rs542009378
NM_002010.3(FGF9):c.-335del rs886050042
NM_002010.3(FGF9):c.-452A>T rs886050041
NM_002010.3(FGF9):c.-585dup rs886050040
NM_002010.3(FGF9):c.-767G>C rs796479555
NM_002010.3(FGF9):c.-796C>T rs549054241
NM_002010.3(FGF9):c.11T>C (p.Leu4Ser)
NM_002010.3(FGF9):c.184A>G (p.Arg62Gly) rs1555223925
NM_002010.3(FGF9):c.296G>A (p.Ser99Asn) rs121918322
NM_002010.3(FGF9):c.430T>C (p.Trp144Arg)
NM_002010.3(FGF9):c.516G>T (p.Pro172=) rs201876493

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.