Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs796052243 0.695 0.520 4 122934574 inframe deletion CAA/- delins 54
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs146539065 0.752 0.240 4 25145092 synonymous variant C/T snv 2.8E-05 4.2E-05 34
rs776969714 0.752 0.240 4 25145129 splice acceptor variant -/C delins 4.2E-05 34
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs1554389088 0.807 0.160 7 44243526 missense variant G/A snv 27
rs6314 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs267606670 0.790 0.320 19 41968837 missense variant C/A;T snv 19
rs1043210477 0.701 0.520 3 49358250 missense variant G/A snv 19
rs995922697 0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs34778348 0.742 0.120 12 40363526 missense variant G/A snv 1.7E-03 5.8E-04 15
rs139455627 0.851 0.240 21 44531087 stop gained G/A snv 3.2E-04 2.7E-04 14
rs1569151872 0.851 0.240 21 44509225 frameshift variant GAC/AA delins 14
rs147484110 0.807 0.200 21 43774760 splice acceptor variant C/G snv 1.5E-04 2.7E-04 11
rs113994152 0.790 0.160 17 75522000 missense variant G/T snv 9.0E-04 9.0E-04 11
rs74315442 0.851 0.200 21 43774297 stop gained G/A snv 4.0E-05 2.1E-05 10