Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs10223646
DSE
0.882 0.080 6 116296236 intron variant C/T snv 0.41 4
rs1043307 0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs10514299 0.827 0.120 5 88367793 intron variant C/T snv 0.21 6
rs11030101 0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 10
rs1106634 0.851 0.080 8 20208538 intron variant G/A;C;T snv 0.18 5
rs1176744 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs11904814 0.851 0.080 2 207562074 intron variant T/G snv 0.30 5
rs120074175 0.827 0.080 12 72031544 missense variant G/A snv 1.2E-05 7.0E-06 7
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs12912233 0.851 0.120 15 60974897 intron variant C/T snv 0.38 5
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1415125856 0.827 0.120 11 27658550 splice region variant G/A snv 4.0E-06 2.1E-05 7
rs1545843 0.827 0.120 12 84170289 intron variant G/A snv 0.52 6
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs174697 0.851 0.080 22 19966309 intron variant A/G snv 0.88 5
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43