Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs148735424 1.000 0.120 6 32697982 intergenic variant -/TTCGTC;TTCGTCAGAC delins 1
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs2650000 0.851 0.200 12 120951159 intron variant A/C snv 0.70 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
rs3763313 0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 5
rs1980495 0.925 0.160 6 32379017 intron variant A/C snv 0.24 2
rs4948088 0.925 0.160 7 50959497 intron variant A/C snv 0.96 2
rs1265564 1.000 0.120 12 111270654 non coding transcript exon variant A/C snv 0.30 1
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 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
rs3095340 1.000 0.120 6 30759162 intron variant A/C snv 0.16 1
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs12720356 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 2
rs1893592 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 2
rs241425 0.925 0.160 6 32837132 intron variant A/C;G snv 2
rs10770141 1.000 0.120 11 2172610 upstream gene variant A/C;G snv 1
rs3957148 0.925 0.160 6 32714360 upstream gene variant A/C;G snv 0.10 1
rs3134603 0.851 0.360 6 32158225 non coding transcript exon variant A/C;G;T snv 4
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs3094061 0.925 0.160 6 30353412 downstream gene variant A/C;T snv 2
rs3094682 1.000 0.120 6 31296684 intron variant A/C;T snv 1