Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1912804
WWOX
0.790 0.080 16 78592686 intron variant C/G;T snv 9
rs3764340
WWOX
0.807 0.280 16 78432540 missense variant C/G snv 7.1E-02 7.4E-02 9
rs12918952
WWOX
0.851 0.120 16 78386878 missense variant G/A;C;T snv 7
rs12716852
WWOX
16 78154841 intron variant G/A snv 0.57 4
rs730882215
WWOX
0.882 0.040 16 78424869 splice acceptor variant G/A snv 4.0E-06 4
rs756762196
WWOX
0.851 0.120 16 78425054 stop gained C/G;T snv 1.6E-05 4
rs383362
WWOX ; MAF
0.882 0.080 16 79211923 missense variant G/T snv 0.44 0.46 4
rs12828
MAF ; WWOX
0.882 0.080 16 79212426 3 prime UTR variant G/A;C snv 3
rs11545028
WWOX
1.000 0.080 16 78099774 5 prime UTR variant C/T snv 0.30 0.28 3
rs11644322
WWOX
0.925 0.120 16 79005703 intron variant C/T snv 0.22 3
rs2345443
WWOX
16 78191736 intron variant A/C;G snv 3
rs587777248
WWOX
0.882 0.040 16 78108475 stop gained C/A;T snv 1.6E-05; 8.0E-06 3
rs1351213477
WWOX ; MAF
1.000 0.080 16 79211708 stop gained C/G;T snv 4.0E-06; 1.2E-05 3
rs1057517846
WWOX
1.000 16 78108446 stop gained G/A snv 2
rs1060502727
WWOX
0.925 0.040 16 78115155 splice donor variant G/C;T snv 4.0E-06 2
rs113496184
WWOX
16 79006207 intron variant G/C;T snv 2
rs1164465811
WWOX
1.000 16 78425056 splice donor variant G/A;C;T snv 4.0E-06 2
rs12716850
WWOX
16 78154006 intron variant A/C;G snv 2
rs1567542020
WWOX
0.925 0.040 16 78386926 stop gained G/T snv 2
rs201008667
WWOX
0.925 0.040 16 78109819 stop gained C/G;T snv 3.2E-05; 3.6E-05 2
rs34592201
WWOX
0.925 0.040 16 78229190 intron variant G/A snv 0.12 2
rs8056446
WWOX
16 78154599 intron variant G/A;C snv 2
rs878855021
WWOX
0.925 0.040 16 78425043 stop gained C/G snv 2
rs9926344
WWOX
1.000 0.080 16 78986883 intron variant G/A;C;T snv 2
rs73569323
MAF ; WWOX
1.000 0.080 16 79211868 missense variant C/T snv 4.7E-02 7.9E-02 1