Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 10
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 7
rs9392504 0.827 0.120 6 412802 downstream gene variant G/A snv 0.44 7
rs9880772 0.827 0.240 3 27736288 intergenic variant G/A snv 0.59 5
rs13069553 0.851 0.200 3 169790484 upstream gene variant A/G snv 0.21 4
rs305061 0.851 0.280 16 85942053 intron variant C/A;T snv 4
rs4240807 0.851 0.160 16 85951755 downstream gene variant A/C snv 0.76 4
rs9378805 0.851 0.280 6 417727 intergenic variant A/C snv 0.36 4
rs9392017 0.851 0.160 6 442357 intergenic variant G/A;C snv 4
rs1679013 0.882 0.160 9 22206988 intron variant C/A;T snv 0.43 3
rs7941765 0.882 0.160 11 128629105 intron variant T/C snv 0.66 3
rs1036935 0.925 0.120 18 50317164 upstream gene variant A/G;T snv 2
rs1359742 0.925 0.120 9 22336997 intergenic variant G/C;T snv 2
rs1476569 0.925 0.120 4 113777540 intergenic variant A/G snv 0.34 2
rs2511713 0.925 0.120 8 102565637 downstream gene variant A/G snv 0.25 2
rs2511714 0.925 0.120 8 102566646 regulatory region variant T/G snv 0.41 2
rs391023 0.925 0.120 16 85894208 upstream gene variant C/T snv 0.48 2
rs391855 0.925 0.120 16 85895015 upstream gene variant A/T snv 0.52 2
rs4368253 0.925 0.120 18 59955055 TF binding site variant T/A;C snv 2
rs57214277 0.925 0.120 4 184333619 downstream gene variant C/T snv 0.33 2
rs674313 0.925 0.120 6 32610305 intergenic variant C/T snv 0.29 2
rs7169431 0.925 0.200 15 56048698 intergenic variant A/G;T snv 2
rs7254272 0.925 0.120 19 4069121 upstream gene variant G/A snv 0.31 2
rs77551289 0.925 0.120 18 63121512 downstream gene variant A/G snv 6.0E-02 2
rs7944004 0.925 0.120 11 2289922 intergenic variant T/G snv 0.48 2