Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 16
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs116909374 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 11
rs13293512 0.763 0.360 9 94167461 intron variant T/C snv 0.24 11
rs9302752 0.925 0.120 16 50685192 upstream gene variant T/C snv 0.68 2
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs2622621 0.851 0.240 4 88109768 intron variant C/A;G snv 6
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 12
rs2228468 0.882 0.120 3 42865620 missense variant A/C;T snv 0.43; 8.3E-03 6
rs653765 0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45 10
rs514049 0.827 0.160 15 58750164 intron variant C/A snv 0.57 6
rs61573157 0.882 0.160 10 70760503 missense variant C/T snv 8.6E-02 7.5E-02 6
rs12774070 0.925 0.120 10 70753879 missense variant C/A;G snv 0.23 0.19 4
rs1130233 0.742 0.480 14 104773557 synonymous variant C/T snv 0.30 0.23 13
rs2071676 0.925 0.120 9 35674056 missense variant G/A snv 0.37 0.30 4
rs2064863 0.925 0.120 20 56387716 intron variant T/A;C;G snv 4
rs11886868 0.752 0.280 2 60493111 intron variant C/T snv 0.65 12
rs4671393 0.790 0.400 2 60493816 intron variant A/C;G snv 11
rs1800477 0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 12
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 34
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs3748093 0.925 0.120 7 140800651 intron variant T/A snv 1.5E-02 4