Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1818879 0.827 0.120 7 22733108 downstream gene variant G/A;C snv 7
rs2253206 0.851 0.080 2 207527254 intron variant A/G snv 0.47 6
rs28386840 0.827 0.080 16 55652906 upstream gene variant T/A;C snv 6
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 9
rs6937506 0.807 0.280 6 132578260 intergenic variant G/A snv 0.25 7
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs776943620
ACE
0.851 0.120 17 63477287 missense variant G/A snv 2.1E-05 7
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs174697 0.851 0.080 22 19966309 intron variant A/G snv 0.88 5
rs749437638 0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05 14
rs1106634 0.851 0.080 8 20208538 intron variant G/A;C;T snv 0.18 5
rs61888800 0.851 0.080 11 27700731 5 prime UTR variant G/T snv 0.19 5
rs11030101 0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 10
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1415125856 0.827 0.120 11 27658550 splice region variant G/A snv 4.0E-06 2.1E-05 7
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs794727961 0.851 0.080 12 2512979 missense variant G/A snv 5
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs528732638 0.851 0.120 18 26940224 intron variant A/-;AA;AAA;AAAA delins 5
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249