Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5522 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1044396 0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs324981 0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs279827 4 46332685 splice region variant A/G;T snv 0.44 0.41 2
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs279858 0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs6296 0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs669 0.851 0.080 12 9079672 missense variant T/C snv 0.31 0.33 7
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs821616 0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 13
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs35369693 1 206116696 missense variant C/G;T snv 4.3E-02 2
rs12936511 0.925 0.080 17 45807036 synonymous variant C/T snv 3.1E-02 3.0E-02 5
rs1801028 0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs1799921 5 63961638 missense variant T/C snv 9.4E-03 9.3E-03 2
rs1800014 0.776 0.200 20 4699875 missense variant G/A snv 8.0E-03 2.2E-03 11
rs1800044 0.827 0.200 5 63961061 missense variant C/A snv 3.7E-03 3.8E-03 8
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs1799920 5 63961656 missense variant C/G;T snv 3.2E-04 2
rs74315457 0.851 0.160 22 50626976 missense variant A/C snv 2.3E-04 2.8E-04 6