Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2715555 0.925 0.080 17 40388372 downstream gene variant G/A snv 9.5E-02 2
rs3217304 0.925 0.080 2 98544046 intron variant ACACAC/-;AC;ACAC;ACACACAC;ACACACACAC;ACACACACACAC delins 0.25 2
rs3776944 0.925 0.080 5 179793009 upstream gene variant G/A snv 8.4E-02 2
rs3806448 0.925 0.080 1 111289583 upstream gene variant G/A snv 0.45 2
rs533116 0.925 0.120 11 60860110 upstream gene variant C/T snv 0.28 2
rs900333744 0.925 0.080 9 21440695 missense variant A/G snv 2
rs7081735 1.000 0.080 10 127998792 5 prime UTR variant G/A snv 0.72 1
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1425851607 0.925 0.080 9 21440691 frameshift variant C/- delins 4.2E-06 2
rs61816761 0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs1362834154 0.925 0.080 16 27363681 missense variant C/T snv 8.0E-06 7.0E-06 2
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs555743307 0.695 0.440 16 27342243 missense variant G/A;T snv 3.6E-05; 2.9E-04 20
rs761019455 1.000 0.080 15 81299818 missense variant G/A snv 4.0E-05 2.8E-05 1
rs11575936 0.851 0.200 6 137219288 missense variant C/T snv 1.3E-03 4.1E-04 4
rs55661460 0.882 0.120 5 159320326 missense variant C/T snv 2.2E-03 7.3E-04 3
rs1805014 0.851 0.080 16 27363708 missense variant T/C snv 7.4E-03 1.4E-02 4
rs41347648 0.882 0.080 13 48707418 missense variant A/G snv 1.7E-02 1.7E-02 3
rs569108 0.790 0.200 11 60095631 missense variant A/G snv 4.7E-02 7.3E-02 8
rs3135932 0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11 23
rs11650354 1.000 0.080 17 47744726 intron variant C/A;T snv 0.16 0.15 1
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 31
rs6967330 0.827 0.120 7 106018005 missense variant G/A snv 0.19 0.21 8
rs1538660 0.882 0.080 9 108879545 missense variant G/A snv 0.19 0.22 3
rs9808753 0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17