Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs5029939 0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs7517847 0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs2424913 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs2297630 0.827 0.160 10 44376100 intron variant G/A;T snv 0.21 6
rs266085 0.851 0.200 10 44378805 intron variant C/T snv 0.32 5
rs1467199 1.000 0.120 2 191015776 intron variant C/G;T snv 2
rs80338835 0.925 0.200 22 36282754 stop gained G/A snv 4.0E-06 7.0E-06 3
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs1884444 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 34
rs2230926 0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs35761398 0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs181206 0.742 0.440 16 28502082 missense variant A/G snv 0.28 0.24 16
rs2501432 0.716 0.480 1 23875430 missense variant T/C;G snv 0.62 16
rs1050501 0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15
rs200215055 0.742 0.400 1 161626196 missense variant C/A;G;T snv 1.5E-03; 1.2E-05; 4.0E-06 11
rs4077515 0.763 0.360 9 136372044 missense variant C/A;T snv 4.0E-06; 0.41 11