Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs2927438 0.925 0.080 19 44738850 intergenic variant G/A snv 0.20 6
rs12570088 0.851 0.160 10 58178575 intergenic variant A/G snv 4.1E-02 4
rs541458 0.851 0.080 11 86077309 regulatory region variant C/T snv 0.71 4
rs7294919 0.851 0.080 12 116889787 regulatory region variant T/C snv 0.19 4
rs7910977 0.882 0.160 10 92450119 downstream gene variant C/T snv 0.17 4
rs1992269 0.925 0.080 18 1872316 intron variant C/T snv 0.24 2
rs376465 0.925 0.080 19 22158230 intergenic variant T/C snv 0.46 2
rs498055 0.925 0.080 10 95595157 non coding transcript exon variant C/A;G;T snv 0.39 2
rs11190302 1.000 0.080 10 99873158 downstream gene variant C/T snv 0.37 1
rs11613092 1.000 0.080 12 118455443 intergenic variant C/T snv 7.9E-02 1
rs11622883 1.000 0.080 14 94689439 regulatory region variant T/A snv 0.37 1
rs2279420 1.000 0.080 10 60022189 downstream gene variant A/G snv 8.8E-02 1
rs7856774 1.000 0.080 9 87110354 regulatory region variant T/A;C snv 1
rs7908652 1.000 0.080 10 84032167 intergenic variant C/T snv 0.57 1
rs3764650 0.790 0.200 19 1046521 intron variant T/G snv 0.14 9
rs4147929 0.882 0.120 19 1063444 intron variant A/C;G snv 3
rs770510230 1.000 0.080 19 1058155 stop gained G/T snv 2.0E-05 4.2E-05 1
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs4343
ACE
0.742 0.480 17 63488670 synonymous variant G/A snv 0.53 14
rs4309
ACE
0.925 0.120 17 63482562 synonymous variant C/T snv 0.46 0.36 3
rs754618480
ACE
1.000 0.080 17 63477951 synonymous variant C/T snv 4.1E-06 1
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52