Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs569108 0.790 0.200 11 60095631 missense variant A/G snv 4.7E-02 7.3E-02 8
rs6967330 0.827 0.120 7 106018005 missense variant G/A snv 0.19 0.21 8
rs2664538 0.827 0.200 20 46011586 missense variant A/G snv 6
rs11575936 0.851 0.200 6 137219288 missense variant C/T snv 1.3E-03 4.1E-04 4
rs1805014 0.851 0.080 16 27363708 missense variant T/C snv 7.4E-03 1.4E-02 4
rs1538660 0.882 0.080 9 108879545 missense variant G/A snv 0.19 0.22 3
rs41347648 0.882 0.080 13 48707418 missense variant A/G snv 1.7E-02 1.7E-02 3
rs55661460 0.882 0.120 5 159320326 missense variant C/T snv 2.2E-03 7.3E-04 3
rs1362834154 0.925 0.080 16 27363681 missense variant C/T snv 8.0E-06 7.0E-06 2
rs900333744 0.925 0.080 9 21440695 missense variant A/G snv 2
rs761019455 1.000 0.080 15 81299818 missense variant G/A snv 4.0E-05 2.8E-05 1
rs1207011218 0.742 0.440 2 203870794 synonymous variant C/T snv 12
rs12603332 0.807 0.200 17 39926554 5 prime UTR variant T/C snv 0.49 7
rs71802646 0.882 0.080 12 57111290 5 prime UTR variant ACACACACACACACAC/-;AC;ACAC;ACACAC;ACACACAC;ACACACACAC;ACACACACACAC;ACACACACACACAC;ACACACACACACACACAC;ACACACACACACACACACAC;ACACACACACACACACACACAC;ACACACACACACACACACACACAC;ACACACACACACACACACACACACAC delins 0.32 3
rs7081735 1.000 0.080 10 127998792 5 prime UTR variant G/A snv 0.72 1
rs324015 0.827 0.120 12 57096317 3 prime UTR variant T/C snv 0.76 5
rs4559 0.882 0.080 12 57095865 3 prime UTR variant C/T snv 0.59 3
rs73985228 0.882 0.080 17 39922412 3 prime UTR variant G/C;T snv 3
rs1425851607 0.925 0.080 9 21440691 frameshift variant C/- delins 4.2E-06 2
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12
rs4794067 0.807 0.280 17 47731462 upstream gene variant T/A;C snv 0.25 7
rs928413 0.807 0.120 9 6213387 upstream gene variant G/A;C snv 7
rs10494132 0.851 0.080 1 111289601 upstream gene variant T/C snv 0.26 4
rs2233407 0.882 0.080 14 35405317 upstream gene variant T/A;C snv 3