Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10019658 1.000 0.040 4 34423326 intergenic variant A/G snv 0.22 1
rs12309467 1.000 0.040 12 83644699 intergenic variant C/A;G snv 1
rs148639588 1.000 0.040 1 102806868 intron variant T/C snv 1
rs16886018 1.000 0.040 5 56682224 intergenic variant C/A snv 6.3E-02 1
rs2487032 1.000 0.040 9 104941653 regulatory region variant G/A snv 0.58 1
rs2627761 1.000 0.040 2 55705879 intergenic variant C/T snv 0.84 1
rs3012455 1.000 0.040 6 170132792 upstream gene variant A/G snv 0.94 1
rs327636 1.000 0.040 7 81219506 intergenic variant A/G snv 0.56 1
rs34935520 1.000 0.040 14 60624683 intergenic variant G/A snv 0.45 1
rs35155027 1.000 0.040 14 60628456 intergenic variant G/C;T snv 0.45 1
rs4492904 1.000 0.040 12 70987768 intergenic variant C/A snv 9.9E-02 1
rs56335522 1.000 0.040 2 212893510 intron variant G/A;C;T snv 1
rs58714937 1.000 0.040 22 19869187 regulatory region variant C/T snv 0.26 1
rs6573307 1.000 0.040 14 60331291 TF binding site variant T/A;G snv 1
rs67530707 1.000 0.040 6 36625210 upstream gene variant AC/- delins 1
rs6947612 1.000 0.040 7 117992921 intergenic variant A/G;T snv 1
rs6969706 1.000 0.040 7 116514777 intergenic variant G/C;T snv 1
rs72815193 1.000 0.040 10 93203634 downstream gene variant A/G snv 0.37 1
rs7389781 1.000 0.040 9 35573945 intergenic variant T/A snv 0.67 1
rs3789134 1.000 0.040 2 110922578 intron variant T/C snv 0.31 1
rs59521811 1.000 0.040 4 7908045 intron variant T/C snv 0.38 1
rs6857814 1.000 0.040 4 7914813 intron variant A/G snv 0.57 1
rs9330348 1.000 0.040 4 7882160 intron variant C/G snv 0.43 1
rs2514882 1.000 0.040 8 107263553 intron variant C/T snv 0.85 1
rs76325372 1.000 0.040 5 14837223 intron variant A/C;T snv 1