Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs505151 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 2
rs6689306 0.925 0.080 1 154423470 intron variant A/G snv 0.61 2
rs9970807 0.925 0.080 1 56499992 intron variant C/T snv 0.11 2
rs10909862 1.000 0.040 1 3020251 upstream gene variant G/A;C;T snv 1
rs11204666 1.000 0.040 1 150570652 intron variant C/G;T snv 1
rs11204892 1.000 0.040 1 151795572 upstream gene variant A/G;T snv 1
rs116161686 1.000 0.040 1 210300277 upstream gene variant G/A snv 9.3E-02 1
rs11806316 1.000 0.040 1 115210861 regulatory region variant G/A snv 0.26 1
rs11809443 1.000 0.040 1 228138791 upstream gene variant T/C snv 0.22 1
rs11810571 1.000 0.040 1 151789832 intron variant C/A;G snv 1
rs12753816 1.000 0.040 1 169183350 intron variant C/T snv 0.24 1
rs147055617 1.000 0.040 1 56520631 intron variant A/G snv 8.3E-02 1
rs1692580
SKI
1.000 0.040 1 2226509 upstream gene variant T/A;C snv 1
rs17416285 1.000 0.040 1 56554977 intron variant C/A;G;T snv 1
rs17465982 1.000 0.040 1 222664597 intron variant G/A snv 0.57 1
rs1892094 1.000 0.040 1 169125221 intron variant C/T snv 0.41 1
rs198389 0.776 0.240 1 11859214 upstream gene variant A/G snv 0.39 1
rs2133189 0.925 0.040 1 222641100 intron variant C/T snv 0.56 1
rs2281719 1.000 0.040 1 230161913 intron variant C/T snv 0.45 1
rs2493298 1.000 0.040 1 3409348 intron variant C/A snv 0.14 1
rs2516839 0.732 0.320 1 161043331 5 prime UTR variant C/T snv 0.49 1
rs2843152 1.000 0.040 1 2314131 upstream gene variant C/G snv 0.65 1
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 1
rs34091558 1.000 0.040 1 201917642 intron variant A/- delins 0.25 1
rs35158675 1.000 0.040 1 222656208 intron variant G/A;C snv 1