Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34569203 1.000 0.040 6 27186205 intergenic variant A/C snv 0.14 1
rs34644694 1.000 0.040 1 117274369 intron variant C/A snv 0.70 1
rs3897644 1.000 0.040 18 60061837 intergenic variant C/T snv 0.48 1
rs391236 1.000 0.040 5 103342372 intergenic variant A/G snv 0.24 1
rs4937872 1.000 0.040 11 112956992 upstream gene variant A/G;T snv 1
rs502652 1.000 0.040 5 101043608 intergenic variant C/T snv 0.27 1
rs525773 1.000 0.040 3 136217611 intergenic variant G/A snv 0.51 1
rs57360718 1.000 0.040 4 118015036 intergenic variant T/C snv 0.10 1
rs61991614 1.000 0.040 14 77018366 regulatory region variant G/A snv 0.21 1
rs62081537 1.000 0.040 18 37668124 intron variant T/C snv 0.16 1
rs62096058 1.000 0.040 18 60229853 intergenic variant G/A snv 0.34 1
rs72893199 1.000 0.040 18 37602745 intron variant T/C snv 0.18 1
rs730356 1.000 0.040 2 147779492 intergenic variant T/A snv 0.15 1
rs888415 1.000 0.040 14 74642492 regulatory region variant A/G;T snv 1
rs9966951 1.000 0.040 18 60108063 intergenic variant G/A snv 0.34 1
rs998884 1.000 0.040 2 147782283 intergenic variant A/G snv 0.37 1
rs1922242 0.827 0.120 7 87544351 intron variant A/T snv 0.43 8
rs1202184 0.851 0.120 7 87584585 intron variant C/T snv 0.39 7
rs1401663578
ACE
0.882 0.120 17 63483037 missense variant A/G snv 1.4E-05 4
rs4822492 1.000 0.040 22 24447626 intron variant C/G snv 0.47 4
rs2298383 0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv 11
rs5751876 0.742 0.320 22 24441333 synonymous variant T/C snv 0.54 0.52 16
rs3761422 1.000 0.040 22 24430704 intron variant T/C snv 0.62 4
rs1017730 1.000 0.040 11 47711942 intron variant G/A snv 0.18 1
rs755246809 0.827 0.280 6 135404951 frameshift variant T/- delins 5.9E-04 4.9E-05 7