Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3829365 0.925 0.040 13 37598759 5 prime UTR variant G/A;C snv 4.0E-06; 0.11 3
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs3212254 0.925 0.040 14 24336257 missense variant G/A;T snv 1.2E-05; 7.3E-02 2
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 16
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs3766871 0.790 0.240 1 237614784 missense variant G/A;T snv 4.0E-02 9
rs2230345 0.807 0.160 10 119326585 missense variant A/T snv 3.8E-02 9.0E-02 6
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs1800888 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs7626962 0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 10
rs34376731 0.925 0.040 12 54581014 missense variant C/T snv 4.6E-03 1.9E-02 2
rs150821281 0.827 0.080 12 32878461 missense variant G/A snv 2.3E-03 2.5E-03 7
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36
rs200536955 0.925 0.040 19 35756980 missense variant G/A;T snv 7.0E-04 3
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs535039125 0.851 0.040 19 41004380 missense variant C/T snv 1.1E-04 1.3E-04 5
rs371401403 0.807 0.080 11 47335996 missense variant G/A;T snv 6.8E-05; 7.9E-05 6
rs28763958
DSP
0.882 0.080 6 7558186 missense variant A/G snv 6.4E-05 2.8E-05 3
rs121918080
TTR
0.827 0.240 18 31595128 missense variant G/A;T snv 2.4E-05 6
rs111033560 0.807 0.040 6 118559037 stop gained T/G snv 1.6E-05 9
rs991104525 0.882 0.160 5 78969051 missense variant G/A snv 1.2E-05 7.7E-05 4
rs749303395 0.882 0.040 1 114680329 missense variant G/A;C snv 8.0E-06; 4.0E-06 3
rs567798234 0.851 0.120 1 109625326 missense variant C/T snv 4.1E-06 7.0E-06 5