Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12413578 0.882 0.160 10 9007290 intergenic variant C/G;T snv 4
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs2647044 0.882 0.240 6 32700133 intergenic variant G/A snv 0.10 3
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 12
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 7
rs9268516 0.882 0.200 6 32411712 upstream gene variant C/T snv 0.24 3
rs9275698 0.925 0.160 6 32720196 downstream gene variant A/G snv 0.37 2
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs9372120 0.851 0.280 6 106219660 intron variant T/G snv 0.16 5
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs6908425 0.752 0.320 6 20728500 intron variant T/C snv 0.78 11
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs563558831 0.776 0.320 19 40991226 upstream gene variant T/C snv 7.0E-06 11
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs367732974
F7
0.790 0.360 13 113105788 5 prime UTR variant G/A snv 8.9E-05 2.8E-05 9
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46