Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1137070 0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 9
rs190783615 0.925 0.040 X 142772620 intergenic variant T/C snv 9.3E-03 3
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs737865 0.763 0.240 22 19942598 intron variant A/G snv 0.23 11
rs174697 0.851 0.080 22 19966309 intron variant A/G snv 0.88 5
rs140504 0.882 0.040 22 23285182 missense variant A/G snv 0.81 0.86 3
rs9722 0.776 0.200 21 46599326 3 prime UTR variant G/A snv 0.16; 2.4E-05 0.21 9
rs3746544 0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 10
rs143934587 0.925 0.040 20 19165806 intergenic variant G/A snv 9.1E-03 3
rs183042538 0.925 0.040 20 41197420 intron variant A/T snv 3.2E-02 3
rs3787283 0.882 0.040 20 10303770 intron variant A/G snv 0.34 3
rs6063349 0.925 0.040 20 49065345 intron variant G/A;C;T snv 3
rs10485715 0.925 0.040 20 7279278 intergenic variant T/C snv 5.5E-02 2
rs4810896 0.925 0.040 20 48918761 upstream gene variant A/C;G snv 2
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs10405744 0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs11082011 0.925 0.040 18 37565159 intron variant C/T snv 0.53 3
rs62100776
DCC
0.925 0.040 18 53228263 intron variant A/T snv 0.35 2
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs1415088003
ACE
0.827 0.160 17 63489038 synonymous variant C/T snv 4.0E-06 7
rs3760138 0.807 0.160 17 76467027 intron variant G/A;T snv 6