Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs579459 0.784 0.107 9 133278724 regulatory region variant C/T snp 0.20 17
rs657152 0.821 0.214 None NA snp 0.41 15
rs687289 0.923 0.143 None NA snp 0.39 9
rs13389219 1.000 0.071 2 164672366 C/T snp 0.46 4
rs507666 0.846 0.036 None NA snp 0.17 4
rs10195252 1.000 0.071 2 164656581 intron variant T/C snp 0.47 3
rs8176719 1.000 0.036 9 133257521 frameshift variant T/TC in-del 0.37 0.37 3
rs998584 6 43790159 regulatory region variant C/A snp 0.41 3
rs4072286 1.000 0.036 8 141726333 intergenic variant G/A,T snp 3.2E-05; 0.42 2
rs6905288 0.923 0.036 6 43791136 intergenic variant G/A snp 0.56 2
rs10039217 5 175751872 intergenic variant A/G snp 4.2E-02 1
rs10107366 8 98101459 T/C snp 1.7E-02 1
rs1020410 2 175919410 intergenic variant T/C snp 0.33 1
rs10274047 7 134685727 intron variant T/G snp 0.33 1
rs10744816 12 114276461 regulatory region variant T/C snp 0.39 1
rs11116045 12 83802750 intergenic variant A/G,T snp 0.28 1
rs11154370 6 126846446 intergenic variant A/G,T snp 3.2E-05; 2.6E-02 1
rs1128249 1.000 0.071 2 164672114 intron variant G/C,T snp 0.46 1
rs11715464 3 42868195 intron variant A/G snp 0.30 1
rs11754509 6 55608496 intergenic variant A/G snp 7.1E-02 1
rs11863065 16 82293200 intergenic variant G/A snp 6.7E-02 1
rs11974269 7 21108059 intergenic variant A/C snp 0.16 1
rs12023396 1 231134890 intergenic variant A/G snp 0.21 1
rs12195826 6 2565518 intergenic variant A/G snp 0.65 1
rs12586774 14 25660360 intergenic variant G/T snp 4.6E-02 1