Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10168266 0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs10174238 0.724 0.200 2 191108308 intron variant G/A snv 0.70 14
rs10181656 0.763 0.360 2 191105153 intron variant G/C snv 0.79 9
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs10840759 0.882 0.200 12 8138610 intron variant C/T snv 0.28 3
rs11066301 0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
rs11085725 0.851 0.160 19 10351837 intron variant C/T snv 0.24 4
rs11203203 0.807 0.240 21 42416077 intron variant G/A snv 0.28 9
rs1150753 0.925 0.120 6 32092090 intron variant A/G snv 6.3E-02 2
rs11568821 0.827 0.200 2 241851760 intron variant C/G;T snv 10
rs117026326 0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs1217393 0.851 0.160 1 113891324 intron variant G/A snv 0.42 4
rs12531711 0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs13101828 0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs13238352 0.827 0.240 7 129007888 intron variant C/T snv 9.1E-02 5
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs1341239 0.776 0.360 6 22303975 intron variant A/C snv 0.65 8
rs1457092 0.790 0.320 19 17193427 intron variant C/A snv 0.44 8
rs1480380 0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs1678542 0.790 0.320 12 57574932 intron variant C/G snv 0.42 9
rs17266594 0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 7
rs17581834 0.882 0.120 1 206802774 intron variant T/C snv 4.2E-02 3
rs17860508 0.752 0.360 5 159333192 intron variant TTAGAG/GC delins 11
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140