Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2929973 0.851 0.200 8 133230265 3 prime UTR variant G/T snv 0.85 5
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1360485 0.742 0.320 13 30457747 3 prime UTR variant C/T snv 0.58 16
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs2075786 0.790 0.360 5 1266195 intron variant A/G snv 0.55 8
rs2929970 0.827 0.200 8 133228894 3 prime UTR variant G/A snv 0.52 5
rs763110 0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs12674822 0.851 0.200 8 6531695 intron variant T/G snv 0.49 4
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs20575 0.645 0.440 8 23201811 missense variant C/G snv 0.54 0.44 29
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs791588 0.851 0.200 10 6047379 intron variant G/T snv 0.40 4
rs2847297 0.827 0.200 18 12797695 intron variant A/G snv 0.40 5
rs11137037 0.851 0.200 8 6538661 intron variant A/C snv 0.40 4
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 17