Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4359426 0.925 0.120 16 57358821 missense variant A/C;T snv 0.92 0.94 3
rs2243191 1.000 0.040 1 206842612 missense variant T/C;G snv 0.71; 5.5E-06 2
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs2255301
CD4
0.925 0.160 12 6800276 intron variant T/C snv 0.59 0.61 3
rs7935564 11 5697287 missense variant G/A snv 0.52 0.55 1
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs10929301 2 233755003 splice region variant C/G;T snv 0.48 4
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs396991 0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs4802 11 123057914 synonymous variant A/C;G snv 4.1E-06; 0.32 2
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs2853699 3 39332411 missense variant C/A;G;T snv 4.0E-06; 0.21; 2.8E-05 1
rs179008 0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18 14
rs1800450 0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs2395029 0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 12
rs3135945 1.000 0.200 3 48467567 synonymous variant G/A snv 9.4E-03 4.0E-02 2
rs1800452 3 46373570 missense variant G/A snv 4.9E-03 1.9E-03 1
rs11568350 0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 9
rs183662584 1.000 3 46373218 missense variant G/A snv 5.2E-04 1.5E-04 2
rs201565523 0.925 0.240 2 218390027 missense variant C/T snv 2.9E-04 7.7E-05 3