Gene: FBXO34 ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10129505
rs10129505
FBXO34
1 14 55309657 intron variant C/T snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs10134317
rs10134317
FBXO34
1 14 55326730 intron variant C/A;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10134339
rs10134339
FBXO34
1 14 55347662 intron variant T/C snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs10140869
rs10140869
FBXO34
1 14 55328565 intron variant G/A snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs10141396
rs10141396
FBXO34
1 14 55350207 intron variant T/G snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs10141552
rs10141552
FBXO34
1 14 55279373 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs10144418
rs10144418
FBXO34
1 14 55350990 synonymous variant T/C snv 0.37 0.36 0.700 1.000 1 2012 2012
dbSNP: rs10146637
rs10146637
FBXO34
2 14 55278092 intron variant G/A snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs10147765
rs10147765
FBXO34
1 14 55361108 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs10150760
rs10150760
FBXO34
1 14 55354830 intron variant A/G snv 0.42 0.700 1.000 1 2012 2012
dbSNP: rs1045002
rs1045002
FBXO34
1 14 55351799 missense variant T/A;G snv 0.38; 4.0E-05 0.700 1.000 1 2012 2012
dbSNP: rs1045004
rs1045004
FBXO34
1 14 55353073 3 prime UTR variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11158034
rs11158034
FBXO34
1 14 55286842 intron variant C/T snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs11621265
rs11621265
FBXO34
1 14 55355377 intron variant G/T snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs11625001
rs11625001
FBXO34
1 14 55291442 intron variant T/C snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs11628437
rs11628437
FBXO34
1 14 55308750 intron variant G/A snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs11851169
rs11851169
FBXO34
1 14 55349214 intron variant G/A snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs11851870
rs11851870
FBXO34
1 14 55349264 intron variant A/C snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs17672950
rs17672950
FBXO34
1 14 55289500 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs17673930
rs17673930
FBXO34
1 14 55341433 intron variant A/G snv 5.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs17674463
rs17674463
FBXO34
1 14 55358145 intron variant A/T snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs17740741
rs17740741
FBXO34
1 14 55295994 intron variant G/C snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs17741542
rs17741542
FBXO34
1 14 55339143 intron variant G/A snv 0.37 0.700 1.000 1 2012 2012
dbSNP: rs17741560
rs17741560
FBXO34
1 14 55339175 intron variant C/T snv 1.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs17741681
rs17741681
FBXO34
1 14 55343997 intron variant A/G snv 5.8E-02 0.700 1.000 1 2012 2012