Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs3025058 0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs6511720 0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs1466535 0.790 0.160 12 57140687 intron variant G/A;C snv 9
rs7025486 0.851 0.040 9 121660124 intron variant G/A snv 0.28 4