Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
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
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs2254298 0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs7124442 0.827 0.160 11 27655494 3 prime UTR variant C/G;T snv 9
rs9357271 0.776 0.160 6 38398097 intron variant T/C snv 0.38 8
rs4565946 0.827 0.080 12 71942989 intron variant C/A;G;T snv 7
rs25532 0.851 0.160 17 30237152 upstream gene variant G/A snv 6.3E-02 5
rs10042486 0.882 0.040 5 63965502 intron variant C/T snv 0.58 4
rs1059004 0.925 0.040 21 33028155 3 prime UTR variant C/A snv 0.41 4
rs13316193 0.882 0.040 3 8761057 intron variant T/C snv 0.45 4
rs1519480 0.925 0.040 11 27654165 intron variant C/T snv 0.54 4
rs3758987 0.925 0.080 11 113904553 upstream gene variant T/C snv 0.32 4
rs9653711 0.851 0.120 21 33029641 intron variant G/A;C snv 4
rs16965628 0.882 0.040 17 30228407 intron variant G/C snv 0.14 3
rs1805477 0.882 0.080 12 13561795 3 prime UTR variant T/A;C;G snv 3
rs2071592 0.882 0.200 6 31547563 intron variant T/A;C snv 3
rs2097603 0.882 0.040 22 19940569 intron variant G/A;T snv 3
rs2268493 0.882 0.040 3 8759154 intron variant T/C snv 0.25 3
rs6517137 0.882 0.120 21 33028471 3 prime UTR variant T/C snv 0.11 3
rs10070190 0.925 0.040 5 26866262 intergenic variant G/A snv 0.60 2
rs11149058 0.925 0.120 13 76978136 downstream gene variant T/A;C;G snv 2