Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 11
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 7
rs9461799 0.807 0.360 6 32721752 downstream gene variant T/C snv 0.37 6
rs6457620 0.882 0.200 6 32696222 intergenic variant G/C snv 0.52 5
rs9469220 0.827 0.160 6 32690533 TF binding site variant G/A snv 0.53 5
rs2621416 0.882 0.280 6 32774091 intergenic variant T/C snv 0.26 4
rs3129768 0.851 0.240 6 32627306 upstream gene variant G/T snv 0.76 4
rs1086603 0.882 0.120 1 147816164 intergenic variant G/A snv 3.4E-02 3
rs12425451 0.882 0.080 12 3055757 TF binding site variant C/T snv 0.54 3
rs1461347 0.882 0.120 11 37191871 intergenic variant T/C snv 4.5E-02 3
rs16830359 1.000 0.080 1 43130713 intergenic variant G/A;T snv 3
rs17138435 0.882 0.120 11 79481943 TF binding site variant A/C;G snv 1.6E-02 3
rs17167034 0.882 0.120 7 88488811 intron variant A/G snv 1.4E-02 3
rs17754109 0.882 0.120 9 17130158 upstream gene variant C/T snv 4.7E-02 3
rs2647046 0.882 0.200 6 32700559 TF binding site variant A/C snv 0.64 3
rs3115576 0.882 0.200 6 32249073 intergenic variant T/A snv 0.41 3
rs3130311 0.882 0.200 6 32249590 intergenic variant A/G;T snv 3
rs3134926 0.882 0.200 6 32232370 intergenic variant C/A;G snv 3
rs4327572 0.882 0.120 5 25972712 intron variant C/T snv 0.28 3
rs455674 0.882 0.120 6 39768626 regulatory region variant C/G;T snv 3
rs6023560 0.882 0.120 20 54743554 intergenic variant A/C;G;T snv 0.12 3
rs7756262 0.882 0.200 6 32430898 intergenic variant T/A snv 0.38 3
rs9267954 0.882 0.200 6 32245275 regulatory region variant A/C;T snv 3
rs9267971 0.882 0.200 6 32249408 intergenic variant T/C snv 0.41 3