Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662 0.561 0.607 7 95308134 missense variant T/C snp 0.38 0.41 71
rs1799971 0.611 0.500 6 154039662 missense variant A/G snp 0.19 0.12 57
rs854560 0.599 0.500 7 95316772 missense variant A/C,G,N,T snp 0.29 0.29 51
rs1006737 0.679 0.107 12 2236129 intron variant G/A snp 0.37 31
rs53576 0.692 0.107 3 8762685 intron variant A/G,T snp 0.67 23
rs4291
ACE
0.784 0.107 17 63476833 regulatory region variant T/A,C snp 0.64 13
rs6311 0.744 0.214 13 46897343 intergenic variant C/T snp 0.40 13
rs2254298 0.784 0.071 3 8760542 intron variant G/A snp 0.15 11
rs4746 0.769 0.250 6 38682852 missense variant T/A,G snp 0.36 0.38 10
rs2000813 0.769 0.143 18 49567494 missense variant C/T snp 4.0E-06; 0.27; 4.0E-06 0.23 9
rs2710102 0.923 0.107 7 147877298 intron variant A/G,T snp 0.56 7
rs121917893 0.846 0.143 X 71167508 missense variant C/T snp 7
rs301430 0.846 0.071 9 4576680 synonymous variant T/C snp 0.36 0.39 7
rs7794745 0.923 0.036 7 146792514 intron variant A/T snp 0.49 6
rs167771 0.878 0.250 3 114157428 intron variant G/A,T snp 0.66 6
rs28364997 0.821 0.107 5 1403013 missense variant G/A snp 5.3E-04 4.8E-04 6
rs4343
ACE
1.000 0.071 17 63488670 synonymous variant G/A snp 0.53 0.56 5
rs4765905 0.878 0.036 12 2240418 intron variant G/A,C snp 0.37 5
rs7608798 0.878 0.107 2 162033707 intron variant G/A snp 0.34 5
rs3746544 0.846 0.036 20 10306436 3 prime UTR variant G/T snp 0.68 5
rs1449263 1.000 0.071 2 181454574 intergenic variant C/T snp 0.56 4
rs73598374
ADA
0.878 0.071 20 44651586 missense variant C/A,G,T snp 7.1E-06; 6.2E-02 4.3E-02 4
rs3796863 0.878 0.107 4 15848363 intron variant G/T snp 0.41 4
rs1060826 0.878 0.107 17 27762841 synonymous variant T/C snp 0.66 0.66 4
rs62643608 0.923 0.071 X 18575391 frameshift variant TT/T in-del 3