Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1718119 0.689 0.520 12 121177300 missense variant G/A;T snv 0.35; 4.0E-06 21
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs5569 0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs696217 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1033656351 0.827 0.160 12 121232997 missense variant G/A snv 1.6E-05 2.8E-05 7
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237