Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs200349593 1.000 0.040 11 114526440 intron variant -/C;CCACTCTCTTCCTC ins 1
rs17780256 0.827 0.120 17 72646784 3 prime UTR variant A/C snv 0.18 6
rs10775412 0.827 0.120 17 27542007 intron variant A/C snv 0.30 5
rs1551399 0.827 0.120 8 125527723 intron variant A/C snv 0.46 5
rs61802846 0.827 0.120 1 161504083 upstream gene variant A/C snv 8.8E-02 5
rs1517352 0.851 0.160 2 191066738 intron variant A/C snv 0.45 3
rs2382817 0.925 0.040 2 218286495 5 prime UTR variant A/C snv 0.61 3
rs6017342 0.925 0.120 20 44436388 non coding transcript exon variant A/C snv 0.62 2
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 1
rs4598195 1.000 0.040 7 107862996 intergenic variant A/C snv 0.34 1
rs7210086 1.000 0.040 17 72645559 downstream gene variant A/C snv 0.17 1
rs12720356 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 7
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs1893592 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
rs714830 0.827 0.120 6 20624151 intron variant A/C;G snv 0.13 5
rs7195296 0.827 0.120 16 11655918 intergenic variant A/C;G snv 5
rs798502 1.000 0.040 7 2750246 intron variant A/C;G snv 4
rs280519 0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 1
rs4654903 1.000 0.040 1 19874497 intergenic variant A/C;G snv 0.53 1
rs11145763 0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs4672505 0.827 0.120 2 62333197 regulatory region variant A/C;G;T snv 5
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs1728785 0.925 0.120 16 68557327 intron variant A/C;T snv 0.77; 7.8E-06 1
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs4625 0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17