Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs757608 17 61419916 regulatory region variant A/G;T snv 4
rs7697556 4 72649596 intergenic variant T/A;C snv 4
rs7763064 6 142476152 intergenic variant G/A snv 0.38 4
rs11750568 1.000 0.080 5 179108712 downstream gene variant A/G;T snv 3
rs117642368 17 45321692 upstream gene variant G/C snv 6.9E-02 3
rs1582931 5 123321505 intergenic variant G/A;T snv 3
rs1659127 16 14294448 intergenic variant G/A;C;T snv 3
rs1759645 6 34227089 TF binding site variant C/T snv 0.71 3
rs2079795 17 61419288 regulatory region variant T/A;C snv 3
rs2597513 1.000 0.040 3 13514336 regulatory region variant C/T snv 0.88 3
rs2731880 0.925 0.040 5 36603282 upstream gene variant T/C snv 0.52 3
rs2778031 1.000 0.040 9 88220811 intergenic variant T/A;C snv 3
rs2780226 6 34231315 regulatory region variant C/T snv 0.80 3
rs28600726 1.000 0.040 4 158730723 intergenic variant G/A snv 0.53 3
rs4549631 6 126645162 intron variant T/C;G snv 3
rs4580892 6 127088737 intron variant C/T snv 0.32 3
rs4794665 1.000 0.160 17 56772968 intergenic variant A/C;G snv 3
rs6449353 4 18031865 intergenic variant T/C snv 0.26 3
rs710841 4 81228677 intergenic variant C/T snv 0.37 3
rs7534091 1 118321993 intergenic variant A/G snv 0.23 3
rs7713145 1.000 0.040 5 177354208 upstream gene variant G/A snv 0.37 3
rs7742369 6 34197944 TF binding site variant A/G snv 0.30 3
rs7846385 8 77247943 intergenic variant T/C snv 0.23 3
rs7968682 12 65978100 intergenic variant G/T snv 0.56 3
rs8099594 1.000 0.040 18 49464790 upstream gene variant A/C;G;T snv 3