Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs10680577 0.776 0.160 19 40798690 intron variant -/TACT delins 10
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs587778883 0.807 0.200 3 37025648 frameshift variant A/- del 7
rs17103265 0.925 0.080 14 35405503 upstream gene variant A/- delins 3
rs5030625 0.882 0.160 16 68736944 upstream gene variant A/- del 0.80 3
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs4652 0.752 0.200 14 55138318 missense variant A/C snv 4.1E-06; 0.45 0.57 12
rs6498486 0.776 0.200 16 13919809 upstream gene variant A/C snv 0.27 8
rs115797771 0.807 0.080 13 73064505 intron variant A/C snv 5.8E-02 6
rs12304647 0.807 0.160 12 53991163 intron variant A/C snv 0.26 6
rs4796030 0.827 0.120 17 35003131 3 prime UTR variant A/C snv 0.66 6
rs2231231 0.851 0.240 9 33442988 non coding transcript exon variant A/C snv 0.67 0.69 5
rs1917799 0.851 0.120 10 49542929 upstream gene variant A/C snv 0.25 4
rs2709800 0.882 0.120 7 30473155 intron variant A/C snv 0.53 4
rs9972882 0.925 0.080 17 39651445 intron variant A/C snv 0.66 4
rs4635002 0.925 0.080 10 127064415 intron variant A/C snv 0.92 3
rs6882903 0.925 0.080 5 40765760 intron variant A/C snv 2.7E-03 2
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs213210 0.742 0.240 6 33208047 upstream gene variant A/C;G snv 11
rs1042229 0.790 0.280 19 51746419 missense variant A/C;G snv 0.32; 0.13 7
rs5273 0.827 0.080 1 186674636 missense variant A/C;G snv 4.0E-06; 7.6E-03 1.4E-02 6
rs36012910 0.925 0.080 2 25345310 upstream gene variant A/C;G snv 2
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113