Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs2925979 1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs592423 6 139519556 intron variant A/C snv 0.50 5
rs900400 0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 5
rs2590838 3 52588070 intron variant G/A snv 0.55 3
rs6450176 5 54002195 intron variant G/A snv 0.27 3
rs731839 19 33408159 intron variant G/A snv 0.63 3
rs1108842 3 52686064 5 prime UTR variant A/C;G;T snv 0.49; 4.0E-06 2
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 2
rs10447248 5 108580035 intergenic variant A/G snv 0.70 1
rs10794657 1 24299684 intergenic variant A/G snv 0.75 1
rs10937273 0.882 0.160 3 186831906 downstream gene variant G/A snv 0.33 1
rs11168618 12 48539450 intergenic variant C/T snv 0.33 1
rs1187415 12 124006982 intron variant G/C snv 0.60 1
rs11924390 3 186715310 intron variant T/A;C snv 1
rs12051272 0.925 0.120 16 82629683 intron variant G/C;T snv 1
rs1515110 2 226257500 intergenic variant G/A;C;T snv 1
rs1648707 0.925 0.080 3 186833922 intergenic variant A/C snv 0.43 1
rs17366568 0.851 0.200 3 186852664 non coding transcript exon variant G/A snv 8.8E-02 1
rs182052 0.701 0.440 3 186842993 intron variant G/A snv 0.38 1
rs2468677 8 139507274 downstream gene variant G/T snv 0.54 1
rs266717 3 186812695 intron variant T/C;G snv 0.57 1
rs266719 3 186783859 non coding transcript exon variant T/C snv 0.84 1
rs2791553 1 219502700 intergenic variant A/G snv 0.57 1
rs2980879 0.925 0.120 8 125469233 intron variant A/T snv 0.69 1