Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs6296 0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs17561 0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26 23
rs5569 0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs5751876 0.742 0.320 22 24441333 synonymous variant T/C snv 0.54 0.52 16
rs315952 0.763 0.400 2 113132727 missense variant T/A;C snv 4.0E-06; 0.31 10
rs9357271 0.776 0.160 6 38398097 intron variant T/C snv 0.38 8
rs1800044 0.827 0.200 5 63961061 missense variant C/A snv 3.7E-03 3.8E-03 8
rs1805502 0.790 0.200 12 13561247 3 prime UTR variant A/G snv 0.25 7
rs518147 0.807 0.200 X 114584109 5 prime UTR variant C/A;G snv 7
rs61752115 0.807 0.320 2 61048535 missense variant T/C snv 4.0E-06 7
rs1013940 0.827 0.160 2 107992192 missense variant A/G snv 9.3E-02 7.4E-02 6
rs3813929 0.851 0.240 X 114584047 upstream gene variant C/G;T snv 5
rs25532 0.851 0.160 17 30237152 upstream gene variant G/A snv 6.3E-02 5
rs2228079 0.882 0.160 1 203129147 synonymous variant T/G snv 0.31 0.26 4