Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs236918 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2596542 0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs2679757 0.925 0.080 8 102858590 intron variant A/G snv 0.37 2
rs26907 0.882 0.240 5 81069496 intron variant G/A;T snv 3
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs28934571 0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3077 0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs376373278
MPO
0.882 0.120 17 58279015 missense variant G/A;C snv 4.2E-06 3
rs3844942 0.882 0.120 4 189571800 intergenic variant T/C snv 3
rs4074 0.827 0.200 4 73870427 intron variant A/G snv 0.46 6
rs430397 0.763 0.240 9 125238840 intron variant C/T snv 9.1E-02 0.11 9
rs4374383 0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs4646038 0.925 0.080 1 15506705 intron variant C/T snv 7.0E-06 2
rs4646437 0.827 0.200 7 99767460 intron variant G/A snv 0.30 8
rs4656942 0.851 0.160 1 160861258 intron variant G/A;C;T snv 4
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs485618 0.851 0.160 1 160830690 3 prime UTR variant T/A;C;G snv 0.54 4
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4898 0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223