Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1275980031 1.000 0.040 7 103540259 missense variant G/A snv 4.0E-06 2
rs779545541 0.882 0.120 14 66965293 missense variant C/T snv 4.0E-06 5
rs893924483 0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs28934908 0.732 0.280 X 154031409 missense variant G/A;T snv 5.5E-06 23
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs3747334 0.925 0.040 X 5893489 synonymous variant G/A;C;T snv 1.2E-05; 6.7E-03 3
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs4541 1.000 0.040 8 142875277 missense variant G/A;T snv 7.8E-02; 2.0E-05 2
rs750257282 1.000 0.040 11 3038127 missense variant C/G;T snv 3.2E-05 3
rs201551401 0.925 0.040 7 124746694 missense variant C/T snv 6.4E-05 1.4E-05 3
rs141441277 0.882 0.120 X 100689933 missense variant G/A snv 5.6E-04 3.8E-04 5
rs121918799 0.752 0.120 2 166015636 missense variant G/C snv 1.7E-03 1.6E-03 14
rs12037377 1.000 0.040 1 246551218 missense variant G/A snv 3.2E-03 1.6E-03 2
rs3747333 0.925 0.040 X 5893491 missense variant G/A;C;T snv 7.6E-03 3
rs6314 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs4534 0.925 0.240 8 142879686 missense variant C/T snv 8.4E-02 4.1E-02 3
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs237902 0.925 0.040 3 8767498 synonymous variant G/A snv 0.29 0.31 3
rs301430 0.827 0.080 9 4576680 synonymous variant T/C snv 0.36 0.38 7
rs9616915 1.000 0.040 22 50679152 missense variant T/C snv 0.43 0.46 2
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs251684 1.000 0.040 19 48098197 synonymous variant T/C snv 0.61 0.64 2
rs6323 0.807 0.040 X 43731789 synonymous variant G/T snv 0.65 7