Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4782371 1.000 0.040 16 88502423 intron variant T/A;G snv 3
rs1144507 0.925 0.080 11 123729767 missense variant A/C;G;T snv 0.68 2
rs2375981 1.000 0.040 9 2692583 regulatory region variant C/G;T snv 2
rs281860391 0.925 0.080 6 31271690 stop gained C/T snv 2
rs750249283 0.925 0.080 21 42296256 missense variant C/G;T snv 4.0E-06; 8.0E-06 2
rs884164 0.925 0.040 19 4521613 upstream gene variant A/G;T snv 2
rs33918808 1.000 0.040 9 104817351 missense variant C/G;T snv 3.5E-02; 4.0E-06 1
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1239681664 0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs567798234 0.851 0.120 1 109625326 missense variant C/T snv 4.1E-06 7.0E-06 5
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs544456198 0.790 0.120 19 11116930 missense variant G/T snv 8.0E-06 2.8E-05 9
rs552953108
F2
0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 16
rs147377392 0.763 0.120 20 23048144 missense variant A/G snv 1.0E-04 2.8E-04 11
rs12713559 0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 10
rs5742904 0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 22
rs72653706 0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs138880920 1.000 0.040 9 104826957 missense variant C/G snv 3.3E-03 1.8E-03 1
rs1800888 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs1800777 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17