Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs1800630
TNF ; LOC100287329 ; LTA
0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 9
rs763000109
TNF
0.827 0.240 6 31575788 missense variant C/G;T snv 4.1E-06; 1.6E-05 9
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02 7
rs1330189219
LTA ; LOC100287329 ; TNF
0.882 0.080 6 31573570 synonymous variant C/T snv 4.0E-06 5
rs1800750
TNF
0.827 0.280 6 31575186 upstream gene variant G/A snv 1.6E-02 5
rs3093661
TNF
1.000 6 31575981 intron variant G/A snv 3.5E-02 4
rs3093668
TNF
1.000 6 31578718 downstream gene variant G/C snv 3.5E-02 4
rs673
TNF
0.882 0.080 6 31575318 upstream gene variant G/A snv 1.8E-02 4
rs1411364031
TNF
0.882 0.040 6 31577502 missense variant T/C snv 7.0E-06 3
rs548532642
TNF
0.882 0.080 6 31577184 missense variant G/A;T snv 1.6E-05 3
rs1250915035
TNF
0.925 6 31576537 missense variant C/T snv 4.0E-06 2
rs3093664
TNF
6 31576865 intron variant A/G snv 6.9E-02 7.7E-02 2
rs1232013698
TNF
6 31577208 missense variant G/T snv 4.1E-06 1
rs1250554906
TNF
1.000 0.120 6 31576808 missense variant G/A snv 4.1E-06 7.0E-06 1
rs1363819544
TNF
1.000 0.160 6 31577126 synonymous variant A/G snv 7.0E-06 1
rs1400328611
TNF
1.000 0.080 6 31575804 frameshift variant AG/- del 1
rs1418646618
TNF
1.000 0.080 6 31575843 missense variant C/G snv 1.2E-05 7.0E-06 1
rs1454071630
TNF
1.000 0.040 6 31577259 missense variant G/A;T snv 8.1E-06 1
rs281865419
TNF
6 31577157 missense variant C/T snv 8.1E-06 7.0E-06 1