Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11680328 1.000 0.040 2 17856540 intergenic variant T/A snv 0.81 1
rs6782299 0.925 0.080 3 180832914 intron variant G/T snv 0.80 2
rs4800149 0.882 0.040 18 23164290 intron variant C/A snv 0.80 3
rs389883 0.827 0.200 6 31979683 non coding transcript exon variant G/T snv 0.80 2
rs6952006 1.000 0.040 7 8094664 downstream gene variant G/T snv 0.79 2
rs4711350 1.000 0.040 6 33773939 intron variant A/G snv 0.79 1
rs6918354 1.000 0.040 6 25444386 intron variant A/T snv 0.79 1
rs236318 1.000 0.040 1 93584664 intron variant C/G snv 0.79 2
rs12602286 1.000 0.040 17 19333641 intron variant G/T snv 0.79 3
rs2565065 1.000 0.040 8 27470504 intron variant A/G snv 0.79 1
rs7499750 1.000 0.040 16 13655408 intergenic variant A/C snv 0.78 1
rs2182139 0.925 0.040 14 59682515 intron variant T/C snv 0.78 2
rs1625579 0.763 0.160 1 98037378 intron variant G/T snv 0.78 5
rs9815738 1.000 0.040 3 88155583 intron variant T/C snv 0.78 1
rs1198588 1.000 0.040 1 98087276 intergenic variant A/T snv 0.78 1
rs1538774 1.000 0.040 1 243381525 intron variant C/G snv 0.78 1
rs10774037 0.882 0.040 12 2311360 intron variant G/A snv 0.77 2
rs9384900 1.000 0.040 6 114389931 intron variant T/C snv 0.77 1
rs1033394 1.000 0.040 6 114392159 intron variant C/T snv 0.77 1
rs9634624 1.000 0.040 13 91376987 intergenic variant G/A snv 0.77 2
rs10803138 1.000 0.040 1 243391917 intron variant A/G snv 0.77 1
rs4736253 1.000 0.040 8 139342742 intergenic variant C/T snv 0.76 1
rs1075195 1.000 0.040 20 38718108 intergenic variant T/C snv 0.76 1
rs2332700 1.000 0.040 14 71950609 intron variant C/G snv 0.76 2
rs4309187 1.000 0.040 11 113541721 intergenic variant A/C snv 0.76 2