Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10049390 0.776 0.080 3 133982275 intron variant G/A snv 0.67 10
rs10246939 0.851 0.240 7 141972804 missense variant T/C snv 0.49 0.47 6
rs10318 0.882 0.080 15 32733778 3 prime UTR variant C/T snv 0.16 3
rs1042028 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1057910 0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 12
rs1078643 0.776 0.080 17 10803924 missense variant G/A;C snv 10
rs10795668 0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24 17
rs10808555 0.925 0.080 8 127397266 intron variant G/A snv 0.65 6
rs10821907 0.776 0.080 10 50888694 upstream gene variant C/T snv 0.20 12
rs10849433 0.776 0.080 12 6297738 regulatory region variant T/C snv 0.38 10
rs10936599 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs10957057 1.000 0.080 8 58487781 downstream gene variant C/T snv 0.12 1
rs10980628 0.776 0.080 9 110909123 intron variant T/C snv 0.16 10
rs11022858 1.000 0.080 11 13505086 intergenic variant T/A;C snv 1
rs1105879 0.790 0.240 2 233693556 missense variant A/C snv 0.35 0.34 11
rs11087784 0.776 0.080 20 7760329 intergenic variant A/G snv 0.13 10
rs11190164 0.776 0.080 10 99591947 intergenic variant A/G snv 0.19 10
rs11196170 0.776 0.080 10 112962862 intron variant G/A;C snv 10
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 11
rs1126667 0.776 0.280 17 6999441 missense variant A/G snv 0.60 0.62 8
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27