Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs2854744 0.695 0.520 7 45921476 intron variant G/T snv 0.48 20
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs169068 0.742 0.280 16 1079872 missense variant C/T snv 0.54 0.50 12
rs267606541
AIP
0.827 0.160 11 67487147 stop gained C/T snv 5
rs1290398674 0.851 0.240 20 58854075 missense variant G/A;T snv 5
rs104894195
AIP
0.882 0.120 11 67490910 stop gained C/G;T snv 4.0E-06; 1.2E-05 4
rs73637412 0.882 0.160 X 137030751 missense variant C/G;T snv 3.5E-03; 1.5E-03 4
rs763751076 0.925 0.160 2 240875132 missense variant C/T snv 1.2E-05 6.3E-05 3
rs2276020 1.000 0.120 11 67490085 missense variant C/G;T snv 3.4E-02 2
rs121908356 0.925 0.120 11 67490804 stop gained C/A snv 2
rs775888932 1.000 0.120 2 96115223 missense variant C/A;T snv 1
rs142833529 1.000 0.120 12 12718195 missense variant T/A;C;G snv 1.2E-05; 5.3E-04 1
rs760330563 1.000 0.120 8 30180515 missense variant C/T snv 4.0E-06 1
rs765502229 1.000 0.120 14 94116511 missense variant T/C snv 1.6E-05 7.0E-06 1
rs34037914 1.000 0.120 16 1079501 synonymous variant C/T snv 5.9E-02 4.8E-02 1
rs642249 1.000 0.120 16 1079912 synonymous variant A/G snv 0.96 0.96 1