Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs4149056 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs237025 0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs17293632 0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs5063 0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 12