Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs4273729 0.851 0.240 6 32710820 upstream gene variant C/A;G;T snv 5
rs10776934 1.000 0.080 9 135137855 regulatory region variant T/G snv 0.74 1
rs11966728 1.000 0.080 6 131955465 intron variant T/C snv 0.26 1
rs12972991 1.000 0.080 19 39241107 upstream gene variant A/C snv 0.19 1
rs12980602 1.000 0.080 19 39262180 upstream gene variant T/C snv 0.25 1
rs4803223 1.000 0.080 19 39255579 upstream gene variant A/G snv 0.13 1
rs8109886 1.000 0.080 19 39252122 upstream gene variant C/A snv 0.53 1
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2287622 0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 16
rs1863918 0.882 0.160 5 179112381 3 prime UTR variant G/T snv 0.25 4
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs2854116 0.807 0.200 11 116829453 upstream gene variant C/T snv 0.51 7
rs2854117 0.851 0.200 11 116829426 upstream gene variant T/A;C snv 6
rs8878 0.827 0.280 4 76021147 3 prime UTR variant A/C;G snv 5
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs6051702 0.882 0.120 20 3271278 intron variant A/C snv 0.19 3
rs965469 1.000 0.080 20 3400902 intron variant T/C snv 0.20 1
rs2230201
C3
0.882 0.200 19 6713280 synonymous variant C/G;T snv 0.19 3
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs2287886 0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 9
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33