Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3897478 1.000 0.040 1 119908567 downstream gene variant T/C snv 0.17 1
rs3916442 1.000 0.040 5 132033475 intergenic variant G/A snv 0.53 1
rs394522 1.000 0.040 6 166984583 intron variant A/C;G snv 1
rs415890 1.000 0.040 6 166993145 intron variant G/A;C snv 1
rs4286721 1.000 0.040 5 40497502 intron variant G/A snv 0.64 1
rs4495224 0.925 0.040 5 40477413 intron variant C/A snv 0.61 1
rs4676406 0.827 0.120 2 240639691 intergenic variant G/T snv 0.53 1
rs4820425 1.000 0.040 22 41035338 intergenic variant C/A;G;T snv 1
rs495662 1.000 0.040 6 117802987 intergenic variant G/A snv 0.92 1
rs559928 0.827 0.120 11 64382898 intergenic variant T/C snv 0.77 1
rs6426833 0.827 0.120 1 19845367 TF binding site variant G/A snv 0.52 1
rs6669582 1.000 0.040 1 67264372 downstream gene variant A/G snv 0.35 1
rs6856616 1.000 0.040 4 38323415 intergenic variant T/C snv 0.15 1
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 1
rs7015630 1.000 0.040 8 89863690 intergenic variant T/A;C snv 1
rs7186163 1.000 0.040 16 50652646 downstream gene variant A/C snv 0.63 1
rs736289 1.000 0.040 19 33266156 intergenic variant T/C snv 0.47 1
rs7426056 0.807 0.120 2 203747335 regulatory region variant A/G snv 0.81 1
rs7517810 1.000 0.040 1 172884320 intron variant C/T snv 0.29 1
rs7539328 1.000 0.040 1 67266920 downstream gene variant G/A;T snv 1
rs7552167 0.807 0.120 1 24192153 upstream gene variant A/G snv 0.87 1
rs7556897 0.807 0.120 2 227795396 intergenic variant C/G;T snv 1
rs7646366 1.000 0.040 3 49433235 upstream gene variant G/A snv 0.29 1
rs7720838 0.925 0.040 5 40486794 intron variant G/T snv 0.52 1
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 1