Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs221798 0.882 0.040 7 100689872 intron variant C/A;G snv 3
rs221774 0.851 0.080 7 100701361 upstream gene variant A/G;T snv 4
rs506597 0.882 0.040 7 100715797 upstream gene variant A/G snv 0.90 4
rs11191454 0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs7914558 0.851 0.040 10 103016151 intron variant G/A snv 0.40 5
rs11191580 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 12
rs9297357 0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs6738485 0.882 0.040 2 106193504 intron variant C/T snv 0.36 3
rs12871532 0.851 0.040 13 108016199 intergenic variant T/C snv 0.46 5
rs56031956 0.882 0.040 9 108863349 missense variant C/G snv 2.3E-02 2.2E-02 3
rs7959663 0.925 0.040 12 109446562 intron variant G/A;C snv 2
rs77867520 0.882 0.040 4 11186225 intergenic variant C/T snv 7.2E-02 3
rs17158930 0.851 0.040 7 111871082 intron variant A/G snv 0.25 4
rs9577511 0.882 0.040 13 113337508 intron variant A/G snv 0.15 4
rs7939917 0.882 0.040 11 113697374 missense variant C/T snv 2.0E-03 9.2E-03 3
rs26318 0.925 0.040 5 116352208 intron variant C/T snv 0.99 3
rs61945387 0.882 0.040 12 117921609 intron variant A/G snv 7.7E-02 3
rs61123830 0.925 0.040 11 123522138 intron variant G/A snv 0.37 2
rs4870888 0.882 0.040 8 124096736 intron variant T/C snv 0.39 4
rs548181 0.851 0.040 11 125591814 5 prime UTR variant A/G snv 0.83 5
rs201048567 0.882 0.040 7 125615031 intergenic variant CA/- delins 1.0E-05 3
rs137928907 0.882 0.040 12 130827204 missense variant A/C snv 1.4E-02 1.5E-02 3
rs7405404 0.925 0.040 16 13656002 intergenic variant T/A;C snv 3
rs105633 0.882 0.040 5 141945684 synonymous variant T/C;G snv 0.98; 4.0E-06 3
rs141252918 0.882 0.040 6 151506923 intron variant G/A;C snv 4