Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs371194629 0.790 0.320 6 29830804 3 prime UTR variant -/ATTTGT;ATTTGTTCACGCCT;ATTTGTTCATGCCT ins 8
rs148735424 1.000 0.120 6 32697982 intergenic variant -/TTCGTC;TTCGTCAGAC delins 1
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs2650000 0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs316019 0.790 0.360 6 160249250 missense variant A/C snv 0.90 0.89 8
rs3763313 0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 7
rs1058026 0.925 0.120 6 31353908 3 prime UTR variant A/C snv 0.21 5
rs2523987 0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 5
rs3129871 0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 5
rs11721827 0.851 0.200 4 186069983 intron variant A/C snv 0.12 4
rs1265564 1.000 0.120 12 111270654 non coding transcript exon variant A/C snv 0.30 4
rs780229030 0.851 0.280 19 45032710 missense variant A/C snv 4
rs2234694 0.882 0.240 21 31666552 intron variant A/C snv 3.6E-02 3.4E-02 3
rs1980495 0.925 0.160 6 32379017 intron variant A/C snv 0.24 2
rs3095340 1.000 0.120 6 30759162 intron variant A/C snv 0.16 2
rs3135002 1.000 0.120 6 32700662 TF binding site variant A/C snv 0.80 2
rs4948088 0.925 0.160 7 50959497 intron variant A/C snv 0.96 2
rs1217385 1.000 0.120 1 113875583 intron variant A/C snv 0.58 1
rs1428168076
CAT
1.000 0.120 11 34452152 missense variant A/C snv 8.0E-06 7.0E-06 1
rs209473 1.000 0.120 6 32955131 intron variant A/C snv 0.56 1
rs2254193 1.000 0.120 9 16801852 intron variant A/C snv 8.5E-02 1
rs229533 1.000 0.120 22 37191071 intron variant A/C snv 0.50 1
rs439121 1.000 0.120 6 33225090 intergenic variant A/C snv 0.27 1
rs917911 1.000 0.120 12 9753255 3 prime UTR variant A/C snv 0.29 1