Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs2227983 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs4244285 0.695 0.360 10 94781859 synonymous variant G/A;C snv 0.18 18
rs4343
ACE
0.742 0.480 17 63488670 synonymous variant G/A snv 0.53 14
rs1265538677 0.790 0.200 13 46055808 synonymous variant A/G snv 4.0E-06 10
rs869109213 0.790 0.200 7 150997269 intron variant GGGGGTGAGGAAGTCTAGACCTGCTGCG/A delins 10
rs9818870 0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 9
rs1234314 0.790 0.320 1 173208253 upstream gene variant C/A;G snv 7
rs4668123 0.851 0.280 2 169196995 missense variant C/A;G;T snv 6
rs2075252 0.925 0.160 2 169154475 stop gained T/A;C snv 0.76 5
rs1187513719 0.851 0.200 10 94780595 missense variant A/G snv 4.0E-06 4
rs2768759 0.851 0.200 1 156882671 downstream gene variant A/C;G snv 4
rs8048002 0.851 0.320 16 10898131 intron variant T/A;C snv 4
rs822442 0.851 0.160 1 156913423 missense variant C/A;T snv 0.14; 4.0E-06 4