Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11749040 0.827 0.120 5 40396323 regulatory region variant G/A snv 0.15 5
rs11749391 0.827 0.120 5 150849504 intron variant T/C snv 0.21 5
rs11750385 0.827 0.120 5 10521556 intron variant G/A;T snv 5
rs12075255 0.827 0.120 1 206788283 intron variant A/G snv 0.74 5
rs12131796 0.827 0.120 1 200909599 intron variant G/A snv 0.22 5
rs1250573 0.827 0.120 10 79282718 intron variant G/A snv 0.23 5
rs12694846 0.827 0.120 2 230283413 intron variant A/G snv 0.20 5
rs12879003 0.827 0.120 14 35359535 downstream gene variant T/A;G snv 0.43 5
rs1292035 0.827 0.120 17 59912196 intron variant G/A snv 0.16 5
rs12932970 0.827 0.120 16 85970504 intron variant T/C snv 0.29 5
rs12943464 0.827 0.120 17 47612985 intron variant A/T snv 0.45 5
rs12987977 0.827 0.120 2 102358876 intron variant T/G snv 0.31 5
rs13107612 0.827 0.120 4 101818823 intron variant C/T snv 0.31 5
rs1328454 0.827 0.120 20 49823486 intron variant T/C snv 0.57 5
rs140135 0.827 0.120 22 29767846 non coding transcript exon variant C/G snv 0.79 5
rs1405108 0.827 0.120 2 198880294 downstream gene variant C/A snv 0.61 5
rs141992399 0.827 0.120 9 136365140 splice donor variant C/G;T snv 3.3E-03; 4.0E-06 5
rs1525735 0.827 0.120 7 17157947 intron variant C/T snv 0.49 5
rs1551399 0.827 0.120 8 125527723 intron variant A/C snv 0.46 5
rs17229679 0.827 0.120 2 198696033 intron variant A/G snv 3.0E-02 5
rs17622517 0.827 0.120 5 132467845 intron variant T/C snv 5.4E-02 5
rs183686347 0.827 0.120 1 67237759 intron variant G/A snv 4.8E-03 5
rs196941 0.827 0.120 17 64069832 non coding transcript exon variant G/C;T snv 5
rs1992661 0.827 0.120 5 40414887 upstream gene variant G/A snv 0.58 5
rs201014116 0.827 0.120 2 25278036 intron variant C/A snv 6.6E-03 5