Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1008953 1.000 0.040 20 45352086 upstream gene variant T/C snv 0.79 1
rs10405308 1.000 0.040 19 1312729 intergenic variant G/A snv 7.9E-02 1
rs10794648 1.000 0.040 1 24191716 upstream gene variant T/C snv 0.68 1
rs10960680 1.000 0.040 9 12483941 intergenic variant A/C snv 9.4E-02 1
rs11135056 1.000 0.040 5 159260273 upstream gene variant C/T snv 0.27 1
rs114934997 1.000 0.040 5 40370622 intergenic variant C/A;T snv 1
rs118179173 1.000 0.040 6 31367764 intron variant T/A snv 3.0E-03 1
rs12118303 1.000 0.040 1 172705957 intergenic variant T/C snv 0.14 1
rs12458130 1.000 0.040 18 8667063 intergenic variant G/A snv 8.9E-02 1
rs1249564 1.000 0.040 1 160466663 regulatory region variant A/G;T snv 1
rs12580100 1.000 0.040 12 56045425 upstream gene variant A/G snv 0.14 1
rs12650590 1.000 0.040 4 155618869 intergenic variant G/T snv 0.14 1
rs141116007 1.000 0.040 9 133631611 intron variant GAGCTGCTCAAGAGAGAGG/- del 0.44 1
rs1581803 1.000 0.040 1 152619805 downstream gene variant G/T snv 0.58 1
rs17203314 1.000 0.040 18 24457493 upstream gene variant A/G snv 0.11 1
rs1886734 1.000 0.040 1 152618666 downstream gene variant A/C;T snv 1
rs2255323 1.000 0.040 7 113078131 upstream gene variant C/T snv 0.17 1
rs2858881 1.000 0.040 6 32736068 upstream gene variant T/C snv 6.8E-02 1
rs3134774 1.000 0.040 6 31233747 regulatory region variant T/C snv 0.26 1
rs35216181 1.000 0.040 14 105699884 downstream gene variant T/C snv 6.3E-02 1
rs4319543 1.000 0.040 12 122160501 intergenic variant A/C snv 0.35 1
rs4379175 1.000 0.040 5 159377920 intron variant G/T snv 0.36 1
rs4845459 1.000 0.040 1 152631366 intergenic variant C/A;G snv 1
rs514475 1.000 0.040 6 137717768 intron variant A/C snv 0.90 1
rs524149 1.000 0.040 18 24458360 upstream gene variant T/C snv 0.92 1