Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1939697 1.000 0.080 11 100220961 intron variant T/G snv 0.81 1
rs1939707 1.000 0.080 11 100231366 intron variant C/A;G;T snv 1
rs7966317 1.000 0.080 12 100401533 intron variant A/G;T snv 1
rs1887276 1.000 0.080 12 100403707 intron variant A/G snv 0.55 1
rs7965082 1.000 0.080 12 100406415 intron variant C/T snv 0.50 1
rs12712133 1.000 0.080 2 102249813 downstream gene variant A/G snv 0.57 1
rs1598856 1.000 0.080 4 102524958 intron variant A/G snv 0.61 1
rs230534 0.882 0.120 4 102527884 intron variant T/C snv 0.73 3
rs17033015 1.000 0.080 4 102625147 intergenic variant A/C snv 0.65 1
rs7677509 1.000 0.080 4 102628849 downstream gene variant T/C snv 0.55 1
rs7699231 1.000 0.080 4 102628918 downstream gene variant A/G snv 0.55 1
rs7699678 1.000 0.080 4 102628939 downstream gene variant G/A snv 0.55 1
rs11724614 1.000 0.080 4 102629091 downstream gene variant A/G snv 0.55 1
rs7664828 1.000 0.080 4 102630219 downstream gene variant C/T snv 0.55 1
rs7665090 0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 6
rs7690123 1.000 0.080 4 102630602 downstream gene variant T/C snv 0.55 1
rs7665659 1.000 0.080 4 102630661 downstream gene variant C/T snv 0.55 1
rs7665854 1.000 0.080 4 102630752 downstream gene variant C/A snv 0.55 1
rs7690700 1.000 0.080 4 102630911 3 prime UTR variant T/A;C snv 1
rs13112557 1.000 0.080 4 102631096 3 prime UTR variant T/C snv 0.55 1
rs12644381 1.000 0.080 4 102631273 3 prime UTR variant A/G snv 0.55 1
rs1054037 1.000 0.080 4 102631552 3 prime UTR variant C/A;T snv 1
rs4013 1.000 0.080 4 102631656 3 prime UTR variant C/T snv 0.55 1
rs4019 1.000 0.080 4 102631673 3 prime UTR variant G/A snv 0.55 1
rs3194585 1.000 0.080 4 102631933 3 prime UTR variant A/G snv 0.55 1