Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs5516 0.827 0.120 19 50820217 missense variant C/G snv 0.69 0.67 6
rs4898 0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs7579 0.807 0.200 5 42800706 3 prime UTR variant C/T snv 0.31 0.26 6
rs1417938
CRP
0.776 0.320 1 159714396 intron variant T/A;C snv 0.28 10
rs2070863 1.000 0.040 17 1745208 missense variant C/G;T snv 0.24 1
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs1057335 0.827 0.120 17 1754359 missense variant G/A snv 0.22 0.20 5
rs3877899 0.827 0.160 5 42801166 missense variant C/A;T snv 4.0E-06; 0.20 7
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs486055 0.925 0.120 11 102779693 missense variant C/G;T snv 1.2E-05; 0.10 3
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs61758388 0.851 0.360 16 17470454 missense variant C/A;G snv 2.7E-02 4
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs8125581 1.000 0.040 20 46010604 missense variant G/A snv 3.0E-04 3.4E-04 1
rs121917864 0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs2306691 1.000 0.040 12 57145019 missense variant A/G snv 2.0E-05 2.1E-05 1
rs767169659 1.000 0.040 3 123733800 missense variant G/A snv 1.2E-05 1
rs773474756 0.925 0.080 11 102790467 missense variant T/C snv 8.1E-06 2
rs782591769
ELN
1.000 0.040 7 74045237 missense variant G/C snv 8.0E-06 1
rs766407419 1.000 0.040 17 1745008 missense variant T/C snv 8.0E-06 1.4E-05 1
rs201191171 0.925 0.080 20 46013279 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 2