Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs2254546 0.807 0.400 8 11486171 upstream gene variant A/G snv 0.83 6
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs10774625 0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs2280964 0.882 0.200 X 71618204 intron variant C/A;G;T snv 3
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs1050501 0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15
rs10917661 0.882 0.160 1 161671427 stop gained C/T snv 2.8E-05 3
rs396991 0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs7528684 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs7192 0.827 0.200 6 32443869 missense variant T/G snv 0.64 0.61 7
rs1063320 0.752 0.360 6 29830972 3 prime UTR variant C/G;T snv 12
rs1707 0.925 0.120 6 29830833 3 prime UTR variant C/T snv 0.87 2
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs2069705 0.695 0.440 12 68161231 intron variant G/A;C snv 19