Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36
rs113993959 0.677 0.280 7 117587778 stop gained G/A;T snv 8.0E-06; 3.4E-04 25
rs2249825 0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs12252 0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs601338 0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 19
rs74597325 0.708 0.320 7 117587811 stop gained C/G;T snv 6.8E-05 18
rs1045411 0.708 0.360 13 30459095 3 prime UTR variant C/T snv 0.20 18
rs1412125 0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs213950 0.716 0.320 7 117559479 missense variant G/A snv 0.47 0.57 16
rs796051877
GAA
0.807 0.320 17 80110055 splice region variant G/A snv 4.0E-06 11
rs4251961 0.763 0.200 2 113116890 intron variant T/C snv 0.29 10
rs1130866 0.827 0.160 2 85666618 missense variant G/A;C snv 0.50 9
rs2294021 0.776 0.280 X 49249149 intron variant T/A;C snv 0.52 8
rs7309123 0.807 0.280 12 10119994 intron variant G/C snv 0.42 8
rs1131692245 0.925 0.160 19 35844109 missense variant C/T snv 7
rs1057518731 0.807 0.280 17 63833908 splice donor variant C/T snv 7
rs1057518733 0.807 0.280 17 63837439 splice donor variant A/G snv 7
rs1555580263 0.827 0.240 17 63837200 stop gained -/AGGTAGAACCTTATCTGCCATCTTC delins 6
rs17615
CR2
0.827 0.200 1 207473117 missense variant G/A snv 0.26 0.31 5
rs4957796
FER
0.851 0.120 5 109066439 intron variant T/C snv 0.16 5