Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs754388 0.882 0.120 14 92649065 intron variant G/C;T snv 5
rs7655625 1.000 0.040 4 144564763 intron variant T/C;G snv 5
rs2955083 1.000 0.040 3 128242335 intron variant T/A snv 0.89 4
rs8756 0.882 0.200 12 65965972 3 prime UTR variant C/A snv 0.56 4
rs3791979 1.000 0.040 2 217802649 3 prime UTR variant T/A;C;G snv 3
rs57942103 1.000 0.040 8 105501233 intron variant A/C snv 0.25 3
rs10883944 1.000 0.040 10 103891899 intron variant G/T snv 0.31 2
rs1158317 1.000 0.040 6 120626545 intron variant C/T snv 0.58 2
rs12173787 1.000 0.040 6 33767694 downstream gene variant G/C snv 0.51 2
rs12709669 1.000 0.040 18 22227108 intron variant T/G snv 0.56 2
rs13409705 1.000 0.040 2 28613010 intron variant C/G snv 0.15 2
rs17186681 1.000 0.040 15 63696566 intron variant A/T snv 0.16 2
rs17431820 1.000 0.040 16 65094555 intron variant T/G snv 7.3E-02 2
rs2512519 1.000 0.040 11 78241969 intron variant C/T snv 0.18 2
rs3738676 1.000 0.040 1 39525916 3 prime UTR variant G/A;T snv 2
rs4746139 1.000 0.040 10 73647891 synonymous variant A/C snv 0.16 0.14 2
rs56386186 1.000 0.040 14 102193651 intron variant T/C snv 9.7E-02 2
rs59985166 1.000 0.040 1 10662447 intron variant C/T snv 4.9E-02 2
rs7143026 1.000 0.040 14 65784238 intergenic variant A/G snv 0.38 2
rs7449334 1.000 0.040 5 91046595 intron variant G/A;C snv 0.76 2
rs9859058 1.000 0.040 3 156795028 intron variant C/A snv 0.39 2